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L-Valine, N-[(1,1-dimethylethoxy)carbonyl]-, 2-oxo-2-phenylethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

111970-72-0

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111970-72-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 111970-72-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,9,7 and 0 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 111970-72:
(8*1)+(7*1)+(6*1)+(5*9)+(4*7)+(3*0)+(2*7)+(1*2)=110
110 % 10 = 0
So 111970-72-0 is a valid CAS Registry Number.

111970-72-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-Boc-L-valine phenacyl ester

1.2 Other means of identification

Product number -
Other names Boc-Val-OPac

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:111970-72-0 SDS

111970-72-0Relevant academic research and scientific papers

Iridium complexes with P-stereogenic phosphino imidazole ligands: Synthesis, structure and catalysis

álvarez-Yebra, Rubén,Rojo, Pep,Riera, Antoni,Verdaguer, Xavier

, p. 4358 - 4364 (2019/04/25)

The synthesis of optically and diastereomerically pure P-stereogenic phosphine-imidazole ligands is reported. The new ligands contain either a benzoimidazole or a 4-phenylimidazole as a N-donor fragment. The ligands have been coordinated to iridium and th

NOVEL SUBSTITUTED AMIDES OF TRITERPENE DERIVATIVES AS HIV INHIBITORS

-

Page/Page column 23, (2017/02/28)

The present invention relates to compounds of novel substituted amides of triteripene derivatives of formula (I); or pharmaceutically acceptable salts, pharmaceutically acceptable solvates, pharmaceutically acceptable hydrates, tautomers, stereoisomers, prodrugs, compositions or combination thereof, wherein R1, R2, R3, R4, R5, R6, R7, R8, X, Y, Z1, Z2, Z3 and formula (II) are as defined herein. The present invention also relates to,, and pharmaceutical compositions comprising compounds of formula (I) useful for the treatment of viral diseases and particularly HIV mediated diseases.

A novel and efficient method for cleavage of phenacylesters by magnesium reduction with acetic acid

Kokinaki, Stella,Leondiadis, Leondios,Ferderigos, Nikolas

, p. 1723 - 1724 (2007/10/03)

(Equation Presented) In the present study, we use magnesium turnings as a new deprotection reagent for the phenacyl group during orthogonal organic synthesis in the presence of other esters and sensitive protecting groups. By applying the new magnesium turnings/acetic acid deprotection method, phenacyl group can be more easily combined with other protecting groups that are not compatible with the zinc/acetic acid method.

Intramolecular triplet-triplet energy transfer in short flexible bichromophoric amino acids, dipeptides and carboxylic acid diester

Zabadal, Miroslav,Heger, Dominik,Klan, Petr,Kriz, Zdenek

, p. 776 - 796 (2007/10/03)

Efficiencies of the intramolecular triplet-triplet energy transfer (ITET) in various bichromophoric amino acids (glycine, valine, phenylalanine, and sarcosine), dipeptides (glycylglycine, phenylalanylphenylalanine), and a simple diester, with the benzoyl

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