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Pentanoic acid, 4-[[(1,1-dimethylethoxy)carbonyl]amino]-5-hydroxy-, phenylmethyl ester, (4R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

195434-34-5

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195434-34-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 195434-34-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,5,4,3 and 4 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 195434-34:
(8*1)+(7*9)+(6*5)+(5*4)+(4*3)+(3*4)+(2*3)+(1*4)=155
155 % 10 = 5
So 195434-34-5 is a valid CAS Registry Number.

195434-34-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (4R)-4-t-butoxycarbonylamino-5-hydroxypentanoic acid benzyl ester

1.2 Other means of identification

Product number -
Other names Boc-D-Glu(OBzl)-ol

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:195434-34-5 SDS

195434-34-5Relevant academic research and scientific papers

Preparative synthesis of β-amino alcohols from α-amino dicarboxylic acid derivatives

Kirillova, Yu. G.,Baranov,Prokhorov,Esipova,Shvets

experimental part, p. 1315 - 1317 (2010/01/11)

A low-expensive preparative procedure has been developed for the synthesis of protected β-amino alcohols from α-amino dicarboxylic acid derivatives.

Optimization of a coagulation factor VIIa inhibitor found in factor Xa inhibitor library

Sagi, Kazuyuki,Fujita, Koichi,Sugiki, Masayuki,Takahashi, Mitsuo,Takehana, Shunji,Tashiro, Kazumi,Kayahara, Takashi,Yamanashi, Masahiro,Fukuda, Yumiko,Oono, Seiji,Okajima, Akiko,Iwata, Seinosuke,Shoji, Masataka,Sakurai, Kuniya

, p. 1487 - 1496 (2007/10/03)

An inhibitor of the complex of factor VIIa and tissue factor (fVIIa/TF), 2-substituted-4-amidinophenylpyruvic acid 1a, was structurally modified with the aim of increasing its potency and selectivity. The lead compound 1a was originally found in our factor Xa (fXa) inhibitor library on the basis of structural similarity of the primary binding sites of fVIIa and fXa. The design was based on computational docking studies using the extracted active site of fVIIa. Compound 1j was found to inhibit factor VIIa/TF at nanomolar concentration with improved selectivity versus fXa and thrombin and it preferentially prolonged the clotting time in the TF-dependent extrinsic pathway.

AMIDINOPHENYLPYRUVIC ACID DERIVATIVES

-

, (2008/06/13)

An amidinophenylpyruvic acid derivative of the following formula, analogs thereof and pharmaceutically acceptable salts thereof have an excellent antagonistic effect against activated blood coagulation factor VII.

A facile and simple method for the reduction of N-protected amino acids and peptides to the corresponding alcohols

Srivastava, Tumul,Srivastava, Tushar K.,Haq,Katti, Seturam B.

, p. 516 - 517 (2007/10/03)

A practical and chemoselective method for the reduction of N-protected amino acids and peptides including carboxylic acids to their corresponding alcohols is outlined.

An efficient method for the reduction of N-protected amino acids and peptides to the corresponding alcohols

Naqvi,Bhattacharya,Haq

, p. 424 - 425 (2007/10/03)

Reduction of pentachlorophenyl esters of Boc protected amino acids and peptides to the corresponding alcohols is described.

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