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40339-42-2

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40339-42-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 40339-42-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,3,3 and 9 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 40339-42:
(7*4)+(6*0)+(5*3)+(4*3)+(3*9)+(2*4)+(1*2)=92
92 % 10 = 2
So 40339-42-2 is a valid CAS Registry Number.

40339-42-2SDS

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 4-methoxy-N-[(1Z)-phenylmethylene]aniline

1.2 Other means of identification

Product number -
Other names phenylcarboxaldehyde N-(p-methoxyphenyl)imine

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:40339-42-2 SDS

40339-42-2Relevant articles and documents

Arthrobacter sp.: a lipase of choice for the kinetic resolution of racemic arylazetidinone precursors of taxanoid side chains

Anand, Naveen,Kapoor, Munish,Ahmad, Khursheed,Koul, Surrinder,Parshad, Rajinder,Manhas, Kuldip S.,Sharma, Rattan L.,Qazi, Ghulam N.,Taneja, Subhash C.

, p. 1059 - 1069 (2008/01/07)

The native strain of Arthrobacter sp. (MTCC 5125) bearing a lipase has been found to be the most effective in the kinetic resolution of racemic arylazetidinones for producing cis-(3R,4S)-3-acetoxy-1-(4-methoxyphenyl)-4-phenyl-2-azetidinone, cis-(3R,4S)-3-

Allylpalladium umpolung in the three-component coupling synthesis of homoallylic amines

Hopkins, Chad D.,Malinakova, Helena C.

, p. 5971 - 5974 (2007/10/03)

(Chemical Equation Presented) Homoallylic amines and α-amino esters were prepared via a Pd(II)-catalyzed coupling of boronic acids and 1,2-nonadiene with ethyl iminoacetate or aliphatic, aromatic, and heteroaromatic imines. The allylpalladium umpolung was

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