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Benzeneselenenamide, N,N-dimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

57584-85-7

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57584-85-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57584-85-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,5,8 and 4 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 57584-85:
(7*5)+(6*7)+(5*5)+(4*8)+(3*4)+(2*8)+(1*5)=167
167 % 10 = 7
So 57584-85-7 is a valid CAS Registry Number.

57584-85-7SDS

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 N,N-Dimethylphenylselenamide

1.2 Other means of identification

Product number -
Other names N,N-Dimethyl-Se-phenyl-selenohydroxylamine

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:57584-85-7 SDS

57584-85-7Downstream Products

57584-85-7Relevant academic research and scientific papers

1H, 13C, 15N, 17O and 77Se NMR of Seleneamides

Paulmier, Claude,Lerouge, Patrice,Outurquin, Francis,Chapelle, Stella,Granger, Pierre

, p. 955 - 959 (2007/10/02)

Numerous areneseleneamides derived from ammonia, primary and secondary amines and two N,N-bis(aryl-seleno) alkylamines have been studied.The selenenamides bearing an electron-withdrawing substituent on the aromatic moiety are stable.The 1H, 13C and 77Se c

The metathesis of N-silylamines and benzeneselenenyl chloride. An efficient selenenamide synthesis

Back, Thomas G.,Kerr, Russell G.

, p. 308 - 310 (2007/10/02)

The metathesis reactions of N-(trimethylsilyl)dialkylamines with benzeneselenenyl chloride afford high yields of N,N-dialkylselenenamides 1a-1f.Similarly, N-(trimethylsilyl)acetamide produces the unstable N-(phenylseleno)amide 2 in situ while N-(trimethyl

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