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tert-butyl (2S)-4,4,4-trichloro-3-hydroxy-1-phenylbutan-2-yl carbamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1050443-38-3

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1050443-38-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1050443-38-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,5,0,4,4 and 3 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1050443-38:
(9*1)+(8*0)+(7*5)+(6*0)+(5*4)+(4*4)+(3*3)+(2*3)+(1*8)=103
103 % 10 = 3
So 1050443-38-3 is a valid CAS Registry Number.

1050443-38-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl (2S)-4,4,4-trichloro-3-hydroxy-1-phenylbutan-2-yl carbamate

1.2 Other means of identification

Product number -
Other names -

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:1050443-38-3 SDS

1050443-38-3Relevant academic research and scientific papers

General and practical conversion of aldehydes to homologated carboxylic acids

Cafiero, Lauren R.,Snowden, Timothy S.

supporting information; experimental part, p. 3853 - 3856 (2009/07/01)

(Chemical Equation Presented) The reaction of aldehydes with trichloromethide followed by sodium borohydride or sodium phenylseleno(triethyl) borate under basic conditions affords homologated carboxylic acids in high yields. This operationally simple procedure provides a practical, efficient alternative to other homologation protocols. The approach is compatible with sensitive aldehydes including enals and enolizable aldehydes. It also offers convenient access to α-monodeuterated carboxylic acids.

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