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145279-67-0

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145279-67-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 145279-67-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,2,7 and 9 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 145279-67:
(8*1)+(7*4)+(6*5)+(5*2)+(4*7)+(3*9)+(2*6)+(1*7)=150
150 % 10 = 0
So 145279-67-0 is a valid CAS Registry Number.

145279-67-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name [(sec-Butylamino)oxy](phenyl)methanone

1.2 Other means of identification

Product number -
Other names O-benzoyl-N-sec-butylhydroxylamine

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:145279-67-0 SDS

145279-67-0Relevant articles and documents

Rhodium(III)-catalyzed C–H amination of 2-arylquinazolin-4(3H)-one with N-alkyl-O-benzoyl-hydroxylamines

Zhang, Yuanguang,Huang, Jiang,Deng, Zhihong,Mao, Xunchun,Peng, Yiyuan

supporting information, p. 2330 - 2337 (2018/04/09)

N-benzoate alkylamines were used as the aminating agents, a efficient Rh-catalyzed ortho C–H amination of 2-arylquinazolin-4(3H)-one has been reported. The reactions exhibit high efficient and good functional group tolerance. Exclusive 2,6-bis-aminated pr

Transition-metal-free electrophilic amination of arylboroxines

Xiao, Qing,Tian, Leiming,Tan, Renchang,Xia, Ying,Qiu, Di,Zhang, Yan,Wang, Jianbo

supporting information; experimental part, p. 4230 - 4233 (2012/09/22)

A transition-metal-free strategy to construct C(sp2)-N bonds using arylboroxines and O-benzoyl hydroxylamines as coupling partners has been developed. This transformation provides a useful method to access various aromatic amines.

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