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1-Indanone - 10mM in DMSO, high purity , CAS No.83-33-0

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1-Indanone - 10mM in DMSO, high purity , CAS No.83-33-0

5 Citations

COA

Grade & Purity:

10mM in DMSO

Cas Number: 83-33-0
Molecular Weight: 132.16
Beilstein Registry Number: 507957
EC Number: 201-470-1
PubChem CID: 6735

In stock

Item Number

I426156

Grouped product items
SKU	Size	Availability	Price	Qty
I426156-1ml	1ml	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$69.90

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Compound libraries (12325)

Basic Description

Synonyms	1-Indanone \| 83-33-0 \| 2,3-Dihydro-1H-inden-1-one \| Indan-1-one \| INDANONE \| alpha-Indanone \| alpha-Hydrindone \| 2,3-dihydroinden-1-one \| 1H-Inden-1-one, 2,3-dihydro- \| 1-Indone \| Hydrindone \| .alpha.-Indanone \| .alpha.-Hydrindone \| MFCD00003785 \| 2,3-Dihydro-1-indenone \| NSC-2581 \| V70
Specifications & Purity	10mM in DMSO
Storage Temp	Store at -80°C
Shipped In	Ice chest + Ice pads This product requires cold chain shipping. Ground and other economy services are not available.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Benzenoids
  - Class Indanes
    - Subclass Indanones

Kingdom	Organic compounds
Superclass	Benzenoids
Class	Indanes
Subclass	Indanones
Intermediate Tree Nodes	Not available
Direct Parent	Indanones
Alternative Parents	Aryl alkyl ketones Organic oxides Hydrocarbon derivatives
Molecular Framework	Aromatic homopolycyclic compounds
Substituents	Indanone - Aryl alkyl ketone - Aryl ketone - Ketone - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Aromatic homopolycyclic compound
Description	This compound belongs to the class of organic compounds known as indanones. These are compounds containing an indane ring bearing a ketone group.
External Descriptors	an aromatic compound
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

Names and Identifiers

IUPAC Name	2,3-dihydroinden-1-one
INCHI	InChI=1S/C9H8O/c10-9-6-5-7-3-1-2-4-8(7)9/h1-4H,5-6H2
InChIKey	QNXSIUBBGPHDDE-UHFFFAOYSA-N
Smiles	C1CC(=O)C2=CC=CC=C21
Isomeric SMILES	C1CC(=O)C2=CC=CC=C21
WGK Germany	3
Molecular Weight	132.16
Beilstein	507957
Reaxy-Rn	507957
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=507957&ln=

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

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

Analytical Chart:

Chemical and Physical Properties

Flash Point(°F)	231.8 °F
Flash Point(°C)	113℃
Boil Point(°C)	245°C
Melt Point(°C)	42°C
Molecular Weight	132.160 g/mol
XLogP3	1.700
Hydrogen Bond Donor Count	0
Hydrogen Bond Acceptor Count	1
Rotatable Bond Count	0
Exact Mass	132.058 Da
Monoisotopic Mass	132.058 Da
Topological Polar Surface Area	17.100 Å²
Heavy Atom Count	10
Formal Charge	0
Complexity	151.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	0
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. Xie Chao, Lin Longfei, Huang Liang, Wang Zixin, Jiang Zhiwei, Zhang Zehui, Han Buxing. (2021) Zn-Nx sites on N-doped carbon for aerobic oxidative cleavage and esterification of C(CO)-C bonds. Nature Communications, 12 (1): (1-12).
2. Shanshan Jie, Congqiang Yang, Yuan Chen, Zhigang Liu. (2018) Facile synthesis of ultra-stable Co-N-C catalysts using cobalt porphyrin and peptides as precursors for selective oxidation of ethylbenzene. Molecular Catalysis, 458 (1).
3. Bing Xia, Yuanji Gao, Baocheng Ji, Fengwei Ma, Lisheng Ding, Yan Zhou. (2018) Analysis of Compounds Dissolved in Nonpolar Solvents by Electrospray Ionization on Conductive Nanomaterials. JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY, 29 (3): (573–580).
4. Yuan Chen, Shanshan Jie, Congqiang Yang, Zhigang Liu. (2017) Active and efficient Co-N/C catalysts derived from cobalt porphyrin for selective oxidation of alkylaromatics. APPLIED SURFACE SCIENCE, 419 (98).
5. Wu Hua-Lei, Zhang Jian-Dong, Zhang Chao-Feng, Fan Xiao-Jun, Chang Hong-Hong, Wei Wen-Long. (2017) Characterization of Four New Distinct ω-Transaminases from Pseudomonas putida NBRC 14164 for Kinetic Resolution of Racemic Amines and Amino Alcohols. APPLIED BIOCHEMISTRY AND BIOTECHNOLOGY, 181 (3): (972-985).

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