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Glycine, N-[[(3-phenyl-2-propenyl)oxy]carbonyl]-, also known as Z-Gly-OH or Z-glycine, is a chemical compound derived from the amino acid glycine. It features a glycine molecule with a benzyloxycarbonyl (Z) protecting group attached to the amino group. This protecting group is commonly used in peptide synthesis to prevent unwanted side reactions and ensure the correct sequence of amino acids in the final peptide product. Z-Gly-OH is a white crystalline solid that is soluble in organic solvents and plays a crucial role in the synthesis of various peptides and pharmaceuticals.

3742-89-0

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3742-89-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3742-89-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,4 and 2 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3742-89:
(6*3)+(5*7)+(4*4)+(3*2)+(2*8)+(1*9)=100
100 % 10 = 0
So 3742-89-0 is a valid CAS Registry Number.

3742-89-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3-phenylprop-2-enoxycarbonylamino)acetic acid

1.2 Other means of identification

Product number -
Other names Glycine,N-[[(3-phenyl-2-propenyl)oxy]carbonyl]

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:3742-89-0 SDS

3742-89-0Downstream Products

3742-89-0Relevant academic research and scientific papers

(3S, 4R)-3,4-trans-disubstituted azetidin-2-one intermediates

-

, (2008/06/13)

The invention relates to an improved process for the preparation of compounds of formula STR1 or salts thereof, starting from compounds of formulae STR2 via compounds of formulae STR3 in which compounds R1 is hydrogen or lower alkyl, R2 is an organic radical which may carry a functional group which may be protected by a customary protective group R2o, R3 is hydrogen or a customary carboxyl protective group R3o, W is a group which can be replaced by a thiocarboxylic acid radical of formula III, and Z is oxygen or sulfur.

THE CINNAMYLOXYCARBONYL GROUP AS A NEW AMINO-PROTECTING GROUP

Kinoshita, Hideki,Inomata, Katsuhiko,Kameda, Takuo,Kotake, Hiroshi

, p. 515 - 518 (2007/10/02)

A new urethane-type protecting group for amines, cinnamyloxycarbonyl (Coc) group, is described.The cleavage of the Coc group is effectively catalyzed by 5 molpercent of in the presence of formic acid, pyridine, and N-hydroxysuccinimide in ref

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