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138386-62-6

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138386-62-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 138386-62-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,3,8 and 6 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 138386-62:
(8*1)+(7*3)+(6*8)+(5*3)+(4*8)+(3*6)+(2*6)+(1*2)=156
156 % 10 = 6
So 138386-62-6 is a valid CAS Registry Number.

138386-62-6SDS

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 (E)-o-(butadienyl)aniline

1.2 Other means of identification

Product number -
Other names ((E)-2-Buta-1,3-dienyl)-phenylamine

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:138386-62-6 SDS

138386-62-6Downstream Products

138386-62-6Relevant articles and documents

Asymmetric Synthesis of 1-Benzazepine Derivatives via Copper-Catalyzed Intramolecular Reductive Cyclization

Li, Dingxi,Park, Yeji,Yoon, Woojin,Yun, Hoseop,Yun, Jaesook

, p. 9699 - 9703 (2019)

An asymmetric construction of enantioenriched 2,3-substituted-1-benzazepine derivatives containing a cyclic tertiary amine moiety was developed by copper-catalyzed reductive intramolecular cyclization of (E)-dienyl arenes with a tethered ketimine. This pr

Cycloaddition Reactions of Carbodiimides. The First Example of an Intramolecular Diels-Alder Reaction of C=C-Conjugated Carbodiimides

Molina, Pedro,Alajarin, Mateo,Vidal, Angel

, p. 1277 - 1279 (2007/10/02)

An one-pot preparation of α-carbolines and quinindolines from conjugated carbodiimides based on a tandem intramolecular Diels-Alder cycloaddition/oxidative aromatization is described.

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