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58377-40-5

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58377-40-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58377-40-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,3,7 and 7 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 58377-40:
(7*5)+(6*8)+(5*3)+(4*7)+(3*7)+(2*4)+(1*0)=155
155 % 10 = 5
So 58377-40-5 is a valid CAS Registry Number.

58377-40-5SDS

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 tert-butyl N-hydroxy-N-phenylcarbamate

1.2 Other means of identification

Product number -
Other names t-butyl N-hydroxy-N-phenylcarbamate

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:58377-40-5 SDS

58377-40-5Relevant articles and documents

Regioselective installation of fluorosulfate (-OSO2F) functionality into aromatic C(sp2)-H bonds for the construction of: Para-amino-arylfluorosulfates

Fang, Wan-Yin,Zha, Gao-Feng,Zhao, Chuang,Qin, Hua-Li

, p. 6273 - 6276 (2019/06/07)

The construction of para-amino-arylfluorosulfates was achieved through installation of fluorosulfate (-OSO2F) functionality into aromatic C(sp2)-H bonds by the reaction of N-arylhydroxylamine with sulfuryl fluoride (SO2Fs

Palladium-catalyzed coupling of hydroxylamines with aryl bromides, chlorides, and iodides

Porzelle, Achim,Woodrow, Michael D.,Tomkinson, Nicholas C. O.

supporting information; experimental part, p. 233 - 236 (2009/06/20)

The bis-pyrazole phosphine ligand BippyPhos is effective for the palladium-catalyzed cross-coupling of hydroxylamines with aryl bromides, chlorides, and iodides. Reactions proceed smoothly at 80 °C in toluene in the presence of Cs2CO3/sub

Facile procedure for the synthesis of N-aryl-N-hydroxy carbamates

Porzelle, Achim,Woodrow, Michael D.,Tomkinson, Nicholas C. O.

body text, p. 798 - 802 (2009/07/25)

An efficient one-pot procedure for the zinc-mediated reduction of nitroarenes in the presence of chloroformates leading to the corresponding N,O-bisprotected hydroxylamine is described. Reactions proceed smoothly under ambient conditions in THF-water mixt

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