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2-bromo-4-methyl-N-allylaniline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

73396-95-9

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73396-95-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73396-95-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,3,9 and 6 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 73396-95:
(7*7)+(6*3)+(5*3)+(4*9)+(3*6)+(2*9)+(1*5)=159
159 % 10 = 9
So 73396-95-9 is a valid CAS Registry Number.

73396-95-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-bromo-4-methyl-N-allylaniline

1.2 Other means of identification

Product number -
Other names N-allyl-2-bromo-4-methyl-aniline

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:73396-95-9 SDS

73396-95-9Downstream Products

73396-95-9Relevant academic research and scientific papers

Insertion Reaction of 2-Halo- N -allylanilines with K 2S Involving Trisulfur Radical Anion: Synthesis of Benzothiazole Derivatives under Transition-Metal-Free Conditions

Liu, Xin-Yu,Zhao, Yan-Wei,Jiang, Tian,Rao, Weidong,Wang, Shun-Yi

, p. 971 - 977 (2020/12/28)

A synthesis of benzothiazole derivatives through the reaction of 2-halo- N -allylanilines with K 2S in DMF is developed. The trisulfur radical anion S 3· -, which is generated in situ from K 2S in DMF, initiates

One-pot N-alkylation/Heck approach to substituted indoles

Weinrich, Melissa L.,Beck, Hilary P.

scheme or table, p. 6968 - 6972 (2010/02/27)

Here, we report the palladium-catalyzed one-pot N-alkylation/Heck cyclization of anilines to substituted indoles employing Pd(OAc)2/XPhos. The scope and limitations of this methodology will be described.

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