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Benzene, 1-chloro-3-(methoxymethyl)-, also known as 1-chloro-3-(methoxymethyl)benzene or 3-(chloromethyl)anisole, is an organic compound with the chemical formula C8H9ClO. It is a colorless liquid with a molecular weight of 156.61 g/mol. Benzene, 1-chloro-3-(methoxymethyl)- is characterized by the presence of a benzene ring, with a chloromethyl group at the 1-position and a methoxymethyl group at the 3-position. It is used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. Due to its reactivity and potential health hazards, it is important to handle this chemical with proper safety measures and in accordance with relevant regulations.

1515-91-9

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1515-91-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1515-91-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,1 and 5 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1515-91:
(6*1)+(5*5)+(4*1)+(3*5)+(2*9)+(1*1)=69
69 % 10 = 9
So 1515-91-9 is a valid CAS Registry Number.

1515-91-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-chloro-3-(methoxymethyl)benzene

1.2 Other means of identification

Product number -
Other names 3-Chlorbenzyl-methyl-ether

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1515-91-9 SDS

1515-91-9Relevant academic research and scientific papers

Studies in the Cycloproparene Series: Competitive Pathways in the Dehydrohalogenation Route to 2-Halobicyclohepta-1,3,5-trienes

Halton, Brian,Randall, Clifford J.,Gainsford, Graeme J.,Robinson, Ward T.

, p. 475 - 489 (2007/10/02)

The (1α,2β,3α,6α)-2,3,7,7-tetrahalobicycloheptanes (8a-c), whose structures have been determined by X-ray methods, give 2-halobicyclohepta-1,3,5-trienes (5) upon dehydrohalogenation.The 'mixed' halide (8c) and partly labelled (7-13C>-(8b,c) have revealed the presence of competing pathways in these conversions.By comparison, dehydrohalogenations of the (1α,3α,4β,6α)-3,4,7,7-tetrahalobicycloheptanes (3) give unrearranged 3-halobicyclo-hepta-1,3,5-trienes (4).

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