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290836-37-2

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290836-37-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 290836-37-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,0,8,3 and 6 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 290836-37:
(8*2)+(7*9)+(6*0)+(5*8)+(4*3)+(3*6)+(2*3)+(1*7)=162
162 % 10 = 2
So 290836-37-2 is a valid CAS Registry Number.

290836-37-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (3S)-3-tert-butoxycarbonylamino-1,1-dichloro-4-phenyl-2-butanone

1.2 Other means of identification

Product number -
Other names tert-butyl (S)-(1-benzyl-3,3-dichloro-2-oxopropyl)carbamate

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:290836-37-2 SDS

290836-37-2Relevant articles and documents

Synthesis of α-amino-α′, α′-dihaloketones and process for the preparation of β-amino acid derivatives by the use of the same

-

, (2008/06/13)

The present invention provides a commercially profitable process for producing a β-amino acid ester derivative which comprises reacting an α-amino acid ester derivative with a base and a dihalomethane, reacting the same with a lithium amide and an alkylli

Dihalomethylation of N-protected phenylalanine esters

Onishi, Tomoyuki,Otake, Yasuyuki,Hirose, Naoko,Nakano, Takashi,Torii, Takayoshi,Nakazawa, Masakazu,Izawa, Kunisuke

, p. 6337 - 6340 (2007/10/03)

Dihalomethylation of several N-protected amino acid esters gave N-protected α-aminoalkyl-α′-dihalomethylketones, which are useful intermediates for the synthesis of erythro β-amino-α-hydroxycarboxylic acids, in good yield. The dihalomethylketones were successfully converted to N-protected α-aminoalkyl-α′-halomethylketones by selective catalytic hydrogenation.

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