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111865-48-6

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111865-48-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 111865-48-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,8,6 and 5 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 111865-48:
(8*1)+(7*1)+(6*1)+(5*8)+(4*6)+(3*5)+(2*4)+(1*8)=116
116 % 10 = 6
So 111865-48-6 is a valid CAS Registry Number.

111865-48-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name benzyl-(3-methyl-but-2-enylidene)amine

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:111865-48-6 SDS

111865-48-6Relevant articles and documents

α,β-Unsaturated imines via Ru-catalyzed coupling of allylic alcohols and amines

Rigoli, Jared W.,Moyer, Sara A.,Pearce, Simon D.,Schomaker, Jennifer M.

supporting information; experimental part, p. 1746 - 1749 (2012/04/23)

A convenient synthesis of α,β-unsaturated imines requiring only an allylic alcohol, an amine and a Ru catalyst has been developed. The use of large excesses of oxidant and the purification of sensitive intermediates can be avoided.

Thiourea-Catalyzed Enantioselective Hydrophosphonylation of Imines: Practical Access to Enantiomerically Enriched α-Amino Phosphonic Acids

Joly, Guy D.,Jacobsen, Eric N.

, p. 4102 - 4103 (2007/10/03)

Chiral thiourea 1b catalyzes the highly enantioselective hydrophosphonylation of a wide range of N-benzyl imines. The hydrophosphonylation products are readily deprotected by hydrogenolysis, providing access to free α-amino phosphonic acids in highly enantioenriched form. Copyright

Synthesis of β,γ-Unsaturated Amino Acids by the Strecker Reaction

Greenlee, W. J.

, p. 2632 - 2634 (2007/10/02)

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