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5-bromo-2-[(phenylmethyl)amino]benzoic acid methyl ester
Cas No: 1131587-77-3
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10 Milligram
Amadis Chemical Co., Ltd.
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Methyl 2-(benzylaMino)-5-broMobenzoate
Cas No: 1131587-77-3
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Chemical Technology Co.,LTD
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methyl 2-(benzylamino)-5-bromobenzoate
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Finetech Industry Limited
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methyl 2-(benzylamino)-5-bromobenzoate
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Debye Scientific
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1131587-77-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1131587-77-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,3,1,5,8 and 7 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1131587-77:
(9*1)+(8*1)+(7*3)+(6*1)+(5*5)+(4*8)+(3*7)+(2*7)+(1*7)=143
143 % 10 = 3
So 1131587-77-3 is a valid CAS Registry Number.

1131587-77-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name	Methyl 2-(benzylamino)-5-bromobenzoate

1.2 Other means of identification

Product number	-
Other names	-

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:1131587-77-3 SDS

1131587-77-3Upstream product

1131587-77-3Downstream Products

443361-07-7 (2-(benzylamino)-5-bromophenyl)methanol

1131587-77-3Relevant articles and documents

Synthesis of substituted indole from 2-aminobenzaldehyde through [1,2]-aryl shift

Levesque, Patrick,Fournier, Pierre-Andre

supporting information; experimental part, p. 7033 - 7036 (2010/11/18)

A mild, efficient, and simple method for the synthesis of 3-ethoxycarbonylindoles has been developed. Addition of ethyl diazoacetate (EDA) to 2-aminobenzaldehydes cleanly affords the indole core. As opposed to other common approaches for the synthesis of indole, this method displays both excellent functional group tolerance and perfect regiochemical control. This allowed the synthesis of a variety of useful indole building blocks from 2-aminobenzaldehydes derived from readily available anthranilic acids.

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CAS

1131587-77-3