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206537-28-2

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206537-28-2 Usage

General Description

3-(N-BOC)amino-3-(2-nitro-phenyl)-propionic acid is a chemical compound with the molecular formula C14H17NO6. It is commonly used in organic synthesis for the preparation of various pharmaceuticals and bioactive compounds. The compound contains a BOC-protected amino group and a nitro-phenyl group, making it valuable for the development of new drugs and therapeutic agents. Its potential applications include the synthesis of peptides, pharmaceutical intermediates, and other organic compounds. Overall, 3-(N-BOC)amino-3-(2-nitro-phenyl)-propionic acid is a versatile and important chemical in the field of medicinal chemistry and drug development.

Check Digit Verification of cas no

The CAS Registry Mumber 206537-28-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,6,5,3 and 7 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 206537-28:
(8*2)+(7*0)+(6*6)+(5*5)+(4*3)+(3*7)+(2*2)+(1*8)=122
122 % 10 = 2
So 206537-28-2 is a valid CAS Registry Number.
InChI:InChI=1/C14H18N2O6/c1-14(2,3)22-13(19)15-10(8-12(17)18)9-6-4-5-7-11(9)16(20)21/h4-7,10H,8H2,1-3H3,(H,15,19)(H,17,18)

206537-28-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[(2-methylpropan-2-yl)oxycarbonylamino]-3-(2-nitrophenyl)propanoic acid

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

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More Details:206537-28-2 SDS

206537-28-2Downstream Products

206537-28-2Relevant articles and documents

Photolytic control of peptide self-assembly

Bosques, Carlos J.,Imperiali, Barbara

, p. 7530 - 7531 (2003)

Herein, we present a methodology that allows for the temporal control of fibrillization of amyloidogenic peptides. This general approach implements a photolabile linker that connects the amyloidogenic peptide to a fibril-inhibitory unit, in this case, a p

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