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1287287-13-1

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1287287-13-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1287287-13-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,8,7,2,8 and 7 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1287287-13:
(9*1)+(8*2)+(7*8)+(6*7)+(5*2)+(4*8)+(3*7)+(2*1)+(1*3)=191
191 % 10 = 1
So 1287287-13-1 is a valid CAS Registry Number.

1287287-13-1SDS

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-(4-chlorophenylaminomethyl)adamantane-1-carbaldehyde

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:1287287-13-1 SDS

1287287-13-1Downstream Products

1287287-13-1Relevant articles and documents

Arylation of adamantanamines: III.* Palladium-catalyzed arylation of adamantane-1,3-diyldimethanamine and 2,2′-(adamantane-1,3-diyl) diethanamine

Averin,Ulanovskaya,Buryak,Savel'ev,Orlinson,Novakov,Beletskaya

experimental part, p. 30 - 40 (2011/04/26)

Palladium-catalyzed arylation of adamantane-1,3-diyldimethanamine and 2,2′-(adamantane-1,3-diyl) diethanamine with isomeric bromochloro- and dibromobenzenes was studied. The yields of N,N′-diarylation products depend on the initial diamine and dihalobenzene structure. Side reactions were revealed, which reduced the yield of the target products. The arylation of 2,2′-(adamantane-1,3-diyl)diethanamine gives the corresponding N,N′-diaryl derivatives with better yield. The possibility for synthesizing unsymmetrical N,N′-diaryl derivatives of 2,2′- (adamantane-1,3-diyl)diethanamine was demonstrated.

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