Basic Description

Synonyms	1-chloromethyl-4-benzyloxy-benzene \| 4-chloromethyl- \| SCHEMBL703 \| 1-(Benzyloxy)-4-(chloromethyl)benzene \| A840619 \| 4-(Benzyloxy)benzylchloride \| P-(BENZYLOXY)BENZYL CHLORIDE \| 1-chloromethyl-4-benzoxy-benzene \| EINECS 212-648-3 \| FT-0659568 \| benzyl 4-
Specifications & Purity	≥97%
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.
Product Description	Description 4-(Benzyloxy)benzyl chloride acts as a solid support to readily determine the loading of the corresponding polymer-bound acids by direct cleavage. This was determined while studying the coupling of substituted aromatic, heterocyclic, and alkyl carboxylates to the resin.4-(benzyloxy)benzyl chloride is used in the preparation of 4-aryl-3,4-dihydropyrimidine-5-carboxylates (DHPMs) which exhibits a wide spectrum of biological effects. Application 4-(benzyloxy)benzyl chloride is used in the preparation of 4-aryl-3,4-dihydropyrimidine-5-carboxylates (DHPMs) which exhibits a wide spectrum of biological effects.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Benzenoids
  - Class Benzene and substituted derivatives
    - Subclass Benzyl halides

Kingdom	Organic compounds
Superclass	Benzenoids
Class	Benzene and substituted derivatives
Subclass	Benzyl halides
Intermediate Tree Nodes	Not available
Direct Parent	Benzyl chlorides
Alternative Parents	Phenoxy compounds Phenol ethers Alkyl aryl ethers Organochlorides Hydrocarbon derivatives Alkyl chlorides
Molecular Framework	Aromatic homomonocyclic compounds
Substituents	Phenoxy compound - Benzyl chloride - Phenol ether - Alkyl aryl ether - Ether - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Organochloride - Organohalogen compound - Alkyl halide - Alkyl chloride - Aromatic homomonocyclic compound
Description	This compound belongs to the class of organic compounds known as benzyl chlorides. These are organic compounds containing a benzene skeleton substituted with a chloromethyl group.
External Descriptors	Not available
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

Pubchem Sid	488184459
IUPAC Name	1-(chloromethyl)-4-phenylmethoxybenzene
INCHI	InChI=1S/C14H13ClO/c15-10-12-6-8-14(9-7-12)16-11-13-4-2-1-3-5-13/h1-9H,10-11H2
InChIKey	UYQPSKUPEXAQRJ-UHFFFAOYSA-N
Smiles	C1=CC=C(C=C1)COC2=CC=C(C=C2)CCl
Isomeric SMILES	C1=CC=C(C=C1)COC2=CC=C(C=C2)CCl
WGK Germany	3
Molecular Weight	232.71
Reaxy-Rn	882526
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=882526&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
C23151263	Certificate of Analysis	Feb 09, 2023	B471625
C23151580	Certificate of Analysis	Feb 09, 2023	B471625
C23151259	Certificate of Analysis	Feb 09, 2023	B471625
C23151261	Certificate of Analysis	Feb 09, 2023	B471625
C23151262	Certificate of Analysis	Feb 09, 2023	B471625
F2518052	Certificate of Analysis	Feb 09, 2023	B471625

Chemical and Physical Properties

Solubility	Soluble in toluene
Sensitivity	Heat sensitive；Moisture sensitive
Melt Point(°C)	77-79 °C
Molecular Weight	232.700 g/mol
XLogP3	3.600
Hydrogen Bond Donor Count	0
Hydrogen Bond Acceptor Count	1
Rotatable Bond Count	4
Exact Mass	232.065 Da
Monoisotopic Mass	232.065 Da
Topological Polar Surface Area	9.200 Å²
Heavy Atom Count	16
Formal Charge	0
Complexity	181.000
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. Wenhui Dong, Xinyuan Sun, Qianqian Niu, Yun Zhu, Baokang Jin. (2024) Efficient electrochemical synthesis of phenylacetic acid derivatives: Utilizing CO2 for sustainable production. International Journal of Electrochemical Science, 19 (100709).

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SKU	Size	Availability	Price
B471625-1g	1g	5	$84.90
B471625-5g	5g	5	$665.90
B471625-25g	25g	2	$2,152.90

4-(Benzyloxy)benzyl chloride - 97%, high purity , CAS No.836-42-0