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Benzene, (3-methyl-2-nitro-1-butenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

113334-89-7

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113334-89-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 113334-89-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,3,3 and 4 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 113334-89:
(8*1)+(7*1)+(6*3)+(5*3)+(4*3)+(3*4)+(2*8)+(1*9)=97
97 % 10 = 7
So 113334-89-7 is a valid CAS Registry Number.

113334-89-7SDS

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 (3-methyl-2-nitrobut-1-enyl)benzene

1.2 Other means of identification

Product number -
Other names Benzene,(3-methyl-2-nitro-1-butenyl)

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:113334-89-7 SDS

113334-89-7Relevant articles and documents

Dynamic kinetic asymmetric ring-opening/reductive amination sequence of racemic nitroepoxides with chiral amines: Enantioselective synthesis of chiral vicinal diamines

Agut, Juan,Vidal, Andreu,Rodríguez, Santiago,González, Florenci V.

, p. 5717 - 5722 (2013/07/25)

We report a highly diastereoselective synthesis of vicinal diamines by the treatment of nitroepoxides with primary amines and then a reducing agent. When using a chiral primary amine, racemic nitroepoxides are transformed into chiral diamines as a single enantiomers (>95:5 er) through a dynamic kinetic asymmetric transformation (DYKAT). The overall process is a one-pot procedure combining the exposure of nitroepoxides to chiral amines to afford diastereomeric mixtures of aminoimines and subsequent stereoselective imine reduction.

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