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Butanamide, 2-bromo-3,3-dimethyl-N-(triphenylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

190260-61-8

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190260-61-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 190260-61-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,0,2,6 and 0 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 190260-61:
(8*1)+(7*9)+(6*0)+(5*2)+(4*6)+(3*0)+(2*6)+(1*1)=118
118 % 10 = 8
So 190260-61-8 is a valid CAS Registry Number.

190260-61-8SDS

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 2-bromo-3,3-dimethyl-N-tritylbutanamide

1.2 Other means of identification

Product number -
Other names N-triphenylmethyl-2-bromo-3,3-dimethylbutanamide

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:190260-61-8 SDS

190260-61-8Relevant academic research and scientific papers

About 1-triphenylmethyl-3-tert-butylaziridinone and some of its reactions [1]

Lengyel,Cesare,Karram,Taldone

, p. 997 - 1002 (2007/10/03)

A high-yield synthesis of 1-triphenylmethyl-3-tert-butylaziridinone (4), its physical and spectral proper- ties, the limits of its thermal stability, and reactions with methanol, benzylamine and sodium methoxide in methanol are described.

Reactivity of 1,3-di-tert-butylaziridinones with phenyl substituents. A new fragmentation of α-lactams

Shimazu, Masako,Endo, Yasuyuki,Shudo, Koichi

, p. 735 - 744 (2007/10/03)

Several isolable aziridinones with bulky substituents were prepared and their reactions with nucleophiles, i.e., methanol, sodium methoxide and benzylamine, were investigated. A novel fragmentation of aziridinones having a phenyl group on the C3 moiety was found.

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