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162936-33-6

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162936-33-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 162936-33-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,2,9,3 and 6 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 162936-33:
(8*1)+(7*6)+(6*2)+(5*9)+(4*3)+(3*6)+(2*3)+(1*3)=146
146 % 10 = 6
So 162936-33-6 is a valid CAS Registry Number.

162936-33-6SDS

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 tert-butyl 4-aminocinnamate

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:162936-33-6 SDS

162936-33-6Relevant articles and documents

Ionic liquid immobilized palladium nanoparticle-Graphene hybrid as active catalyst for heck reaction

Srivastava, Vivek

, p. 67 - 72 (2015/04/14)

We engineered, graphene based Pd-Nano composites (Pd/RGO) and tested them to catalyze the Heck reaction in [bmim] NTf2 solvent system. High yield, easy product isolation, recycling of the catalytic system and ligand free approach are the main outcomes of this proposed protocol. The proposed protocol was further exploited for the successful synthesis of 3-styryl coumarins in good yield.

2-Aralkynyl and 2-Heteroalkynyl Derivatives of Adenosine-5'-N-ethyluronamide as Selective A2a Adenosine Receptor Agonists

Cristalli, Gloria,Camaioni, Emidio,Vittori, Sauro,Volpini, Rosaria,Borea, Pier Andrea,et al.

, p. 1462 - 1472 (2007/10/02)

A series of new 2-aralkynyl and 2-heteroaralkynyl derivatives of NECA were synthesized and studied in binding and functional assays to assess their potency for the A2a compared to A1 adenosine receptors.Compounds bearing an aromatic

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