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2-Propenoic acid, 3-phenyl-2-[[(phenylmethoxy)carbonyl]amino]-, (Z)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

72015-61-3

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72015-61-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72015-61-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,0,1 and 5 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 72015-61:
(7*7)+(6*2)+(5*0)+(4*1)+(3*5)+(2*6)+(1*1)=93
93 % 10 = 3
So 72015-61-3 is a valid CAS Registry Number.

72015-61-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (Z)-2-benzyloxycarbonylaminocinnamic acid

1.2 Other means of identification

Product number -
Other names Z-ΔPhe-OH

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:72015-61-3 SDS

72015-61-3Relevant academic research and scientific papers

PREPARATION OF ALL THE FOUR DIASTEREOMERS OF β-PHENYLCYSTEINE METHYL ESTER THROUGH CHROMATOGRAPHIC OPTICAL RESOLUTION OF THE 2,2-DIMETHYLTHIAZOLIDINE DERIVATIVES

Nagai, Ukon,Pavone, Vincenzo

, p. 589 - 592 (2007/10/02)

cis- And trans-2,2-dimethyl-4-carbomethoxy-5-phenylthiazolidines prepared from the corresponding erythro- and threo-β-phenylcysteines were resolved into the enantiomers by use of a chiral HPLC column, from which all of the four chiral β-phenylcysteine met

N--ΔE-phenylalanine Ethyl Ester

Nitz, Theodore J.,Holt, Elizabeth M.,Rubin, Byron,Stammer, Charles H.

, p. 2667 - 2671 (2007/10/02)

The synthesis of the title compound (1a) has been accomplished by rearrangement of a vinylic isocyanate, and its configuration was confirmed by X-ray crystallography.The configurational stability of 1a to both acids and bases was investigated, and the NMR

THE SYNTHESES OF N-FREE α-DEHYDROAMINO ACID ESTERS AND N-ACETYL DEHYDRODIPEPTIDE ESTER FROM N-CARBOXY α-DEHYDROAMINO ACID ANHYDRIDE

Shin, Chung-gi,Yonezawa, Yasuchika,Yoshimura, Juji

, p. 1635 - 1638 (2007/10/02)

N-Carboxy α-dehydroamino acid anhydride, derived from N-benzyloxycarbonyl α-dehydroamino acid (DHA) and thionyl chloride, was found to be very useful for the synthesis of N-free DHA ester by alcoholysis and N-acetyl dehydrodipeptide ester by coupling was

The Preparation and Reactions of 2-Benzyloxy-4-benzylideneoxazol-5-one

Jones, John H.,Witty, Michael J.

, p. 858 - 864 (2007/10/02)

The preparation of the title coumpound (4) and a survey of its chemistry are described.Its reactivity towards nucleophiles at C-5 is high compared with that of the corresponding 2-phenyl compound (1), and nucleophilic reagents attact (4) exclusively at th

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