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20914-24-3

20914-24-3

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20914-24-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20914-24-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,9,1 and 4 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 20914-24:
(7*2)+(6*0)+(5*9)+(4*1)+(3*4)+(2*2)+(1*4)=83
83 % 10 = 3
So 20914-24-3 is a valid CAS Registry Number.

20914-24-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name Allylphenylcyanamide

1.2 Other means of identification

Product number -
Other names allyl-phenyl-carbamonitrile

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:20914-24-3 SDS

20914-24-3Downstream Products

20914-24-3Relevant articles and documents

Catalytic Dealkylative Synthesis of Cyclic Carbamates and Ureas via Hydrogen Atom Transfer and Radical-Polar Crossover

Nagai, Takuya,Mimata, Nao,Terada, Yoshihiro,Sebe, Chikayoshi,Shigehisa, Hiroki

supporting information, p. 5522 - 5527 (2020/07/24)

Guided by the transition-metal hydrogen atom transfer and radical-polar crossover concepts, we developed a functional-group-tolerant and scalable method for the synthesis of cyclic carbamates and ureas, which are found in the structures of bioactive compo

Modification of the Tiemann rearrangement: One-pot synthesis of N,N-disubstituted cyanamides from amidoximes

Bakunov, Stanislav A.,Rukavishnikov, Alexey V.,Tkachev, Alexey V.

, p. 1148 - 1159 (2007/10/03)

A three-stage one-pot synthetic procedure for transformation of amidoximes to N,N-disubstituted cyanamides in 70-92% yield is described.

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