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Hydrobenzoin - 98%, high purity , CAS No.492-70-6

7 Citations

COA

Grade & Purity:

≥98%

Cas Number: 492-70-6
Molecular Weight: 214.26
MDL number: MFCD00004499
PubChem CID: 95447

In stock

Item Number

H487118

Grouped product items
SKU	Size	Availability	Price
H487118-250mg	250mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$43.90
H487118-1g	1g	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$110.90
H487118-5g	5g	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$399.90

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Benzene compounds (294)

Basic Description

Synonyms	H0815 \| SY106437 \| EINECS 207-758-3 \| Gemixa \| N'-Hydroxy-3-(trifluoromethyl)benzene-1-carboximidamide \| 1,2-Ethanediol, 1,2-diphenyl-, (R,R)-(.+/-.)- \| FT-0605349 \| MLS001180169 \| CHEBI:50013 \| AB-131/40897135
Specifications & Purity	≥98%
Storage Temp	Store at 2-8°C
Shipped In	Wet ice This product requires cold chain shipping. Ground and other economy services are not available.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Phenylpropanoids and polyketides
  - Class Stilbenes

Kingdom	Organic compounds
Superclass	Phenylpropanoids and polyketides
Class	Stilbenes
Subclass	Not available
Intermediate Tree Nodes	Not available
Direct Parent	Stilbenes
Alternative Parents	Benzene and substituted derivatives Secondary alcohols 1,2-diols Hydrocarbon derivatives Aromatic alcohols
Molecular Framework	Aromatic homomonocyclic compounds
Substituents	Stilbene - Benzenoid - Monocyclic benzene moiety - Secondary alcohol - 1,2-diol - Organic oxygen compound - Hydrocarbon derivative - Aromatic alcohol - Organooxygen compound - Alcohol - Aromatic homomonocyclic compound
Description	This compound belongs to the class of organic compounds known as stilbenes. These are organic compounds containing a 1,2-diphenylethylene moiety. Stilbenes (C6-C2-C6 ) are derived from the common phenylpropene (C6-C3) skeleton building block. The introduction of one or more hydroxyl groups to a phenyl ring lead to stilbenoids.
External Descriptors	a small molecule
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Associated Targets(Human)

ACHE Tclin Acetylcholinesterase (18204 Activities)

Discover Target: ACHE

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

BCHE Tclin Butyrylcholinesterase (7174 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CES2 Tchem Carboxylesterase 2 (583 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CES1 Tchem Acyl coenzyme A:cholesterol acyltransferase (1029 Activities)

Discover Target: CES1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

GNAS Tbio Guanine nucleotide-binding protein G(s), subunit alpha (103405 Activities)

Discover Target: GNAS

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mechanisms of Action

Mechanism of Action	Action Type	target ID	Target Name	Target Type	Target Organism	Binding Site Name	References

Names and Identifiers

IUPAC Name	1,2-diphenylethane-1,2-diol
INCHI	InChI=1S/C14H14O2/c15-13(11-7-3-1-4-8-11)14(16)12-9-5-2-6-10-12/h1-10,13-16H
InChIKey	IHPDTPWNFBQHEB-UHFFFAOYSA-N
Smiles	C1=CC=C(C=C1)C(C(C2=CC=CC=C2)O)O
Isomeric SMILES	C1=CC=C(C=C1)C(C(C2=CC=CC=C2)O)O
Molecular Weight	214.26
Reaxy-Rn	2050813
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2050813&ln=

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

6 results found

Lot Number	Certificate Type	Date	Item
B2524055	Certificate of Analysis	Feb 12, 2025	H487118
B2524062	Certificate of Analysis	Feb 12, 2025	H487118
C2505764	Certificate of Analysis	Feb 12, 2025	H487118
C2505765	Certificate of Analysis	Feb 12, 2025	H487118
B2524052	Certificate of Analysis	Feb 12, 2025	H487118
B2524057	Certificate of Analysis	Feb 12, 2025	H487118

Chemical and Physical Properties

Flash Point(°F)	Not applicable
Flash Point(°C)	Not applicable
Molecular Weight	214.260 g/mol
XLogP3	1.600
Hydrogen Bond Donor Count	2
Hydrogen Bond Acceptor Count	2
Rotatable Bond Count	3
Exact Mass	214.099 Da
Monoisotopic Mass	214.099 Da
Topological Polar Surface Area	40.500 Å²
Heavy Atom Count	16
Formal Charge	0
Complexity	171.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	2
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

Citations of This Product

How to Cite Aladdin Scientific Products?

1. Kong Kejian, Li An-Zhen, Wang Ye, Shi Qiujin, Li Jing, Ji Kaiyue, Duan Haohong. (2023) Electrochemical carbon–carbon coupling with enhanced activity and racemate stereoselectivity by microenvironment regulation. Nature Communications, 14 (1): (1-12).
2. Ya-Nan Gong, Qi-Yu Ma, Ying Wang, Jun-Hui Zhang, You-Ping Zhang, Rui-Xue Liang, Bang-Jin Wang, Sheng-Ming Xie, Li-Ming Yuan. (2023) Preparation of Chiral Porous Organic Cage Clicked Chiral Stationary Phase for HPLC Enantioseparation. MOLECULES, 28 (7): (3235).
3. Ming-Yu Qi, Qiong Lin, Zi-Rong Tang, Yi-Jun Xu. (2022) Photoredox coupling of benzyl alcohol oxidation with CO2 reduction over CdS/TiO2 heterostructure under visible light irradiation. APPLIED CATALYSIS B-ENVIRONMENTAL, 307 (121158).
4. Yue-Hua Li, Ming-Yu Qi, Zi-Rong Tang, Yi-Jun Xu. (2022) Coupling Organic Synthesis and Hydrogen Evolution over Composite WO3/ZnIn2S4 Z-Scheme Photocatalyst. Journal of Physical Chemistry C, 126 (4): (1872–1880).
5. Lan Yuan, Yue-Hua Li, Zi-Rong Tang, Jinlong Gong, Yi-Jun Xu. (2020) Defect-promoted visible light-driven CC coupling reactions pairing with CO2 reduction. JOURNAL OF CATALYSIS, 390 (244).
6. Nengchao Luo, Tingting Hou, Shiyang Liu, Bin Zeng, Jianmin Lu, Jian Zhang, Hongji Li, Feng Wang. (2020) Photocatalytic Coproduction of Deoxybenzoin and H2 through Tandem Redox Reactions. ACS Catalysis, 10 (1): (762–769).
7. Meifang Cao, Yuqiao Ma, Tao Ruan, Lifeng Li, Bo Chen, Xueqing Qiu, Di Fan, Xinping Ouyang. (2024) Highly efficient hydrogenolysis of lignin into monophenol over an atomically dispersed platinum catalyst. CHEMICAL ENGINEERING JOURNAL, 485 (150020).

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