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39533-32-9

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39533-32-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 39533-32-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,5,3 and 3 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 39533-32:
(7*3)+(6*9)+(5*5)+(4*3)+(3*3)+(2*3)+(1*2)=129
129 % 10 = 9
So 39533-32-9 is a valid CAS Registry Number.

39533-32-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl α-phenyl-α-isocyanoacetate

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:39533-32-9 SDS

39533-32-9Relevant articles and documents

Novel multicomponent reaction for the combinatorial synthesis of 2-imidazolines

Bon, Robin S.,Hong, Chongen,Bouma, Marinus J.,Schmitz, Rob F.,De Kanter, Frans J. J.,Lutz, Martin,Spek, Anthony L.,Orru, Romano V. A.

, p. 3759 - 3762 (2003)

(Matrix presented) The three-component condensation between an amine, an aldehyde, and an α-acidic isocyanide efficiently provides substituted 2-imidazolines in a one-pot reaction under mild conditions.

Catalytic enantioselective Michael addition of α-aryl-α- isocyanoacetates to vinyl selenone: Synthesis of α,α-disubstituted α-amino acids and (+)- and (-)-trigonoliimine A

Buyck, Thomas,Wang, Qian,Zhu, Jieping

, p. 12714 - 12718 (2013/12/04)

Be like Mike: The title reaction in the presence of the catalyst 1 afforded Michael adducts in excellent yields and enantioselectivities. The adducts were readily converted into α,α′-disubstituted α-amino acids. The enantioselective total synthesis of bot

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