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Carbamic acid, [2-oxo-1-(phenylmethyl)-2-(2-pyridinylamino)ethyl]-, 1,1-dimethylethyl ester, (S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88932-67-6

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88932-67-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88932-67-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,9,3 and 2 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 88932-67:
(7*8)+(6*8)+(5*9)+(4*3)+(3*2)+(2*6)+(1*7)=186
186 % 10 = 6
So 88932-67-6 is a valid CAS Registry Number.

88932-67-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-<<N-(tert-butyloxycarbonyl)-L-phenylalanyl>amino>pyridine

1.2 Other means of identification

Product number -
Other names [(S)-2-Phenyl-1-(pyridin-2-ylcarbamoyl)-ethyl]-carbamic acid tert-butyl ester

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:88932-67-6 SDS

88932-67-6Relevant academic research and scientific papers

Discovery of novel dual-action antidiabetic agents that inhibit glycogen phosphorylase and activate glucokinase

Zhang, Lei,Chen, Xiaojie,Liu, Jun,Zhu, Qingzhang,Leng, Ying,Luo, Xiaomin,Jiang, Hualiang,Liu, Hong

, p. 624 - 639 (2013/02/21)

Dual-target-directed agents simultaneously inhibiting glycogen phosphorylase (GP) and activating glucokinase (GK) could decelerate the inflow of glucose from glycogenolysis and accelerate the outflow of glucose in the liver, therefore allow for a better control over hyperglycaemia in a synergetic manner. A series of hybrid compounds were designed by structure-assisted and ligand-based strategies. In vitro bioassays found two novel compounds (1j, 6g) worthy of further optimization on balance of dual action to GP and GK. In addition, for single-target activity, two compounds exhibited more potent GP inhibitory activity and four compounds showed better GK activation than their corresponding references.

Primary amine-metal Lewis acid bifunctional catalysts based on a simple bidentate ligand: Direct asymmetric aldol reaction

Daka, Philias,Xu, Zhenghu,Alexa, Alexandru,Wang, Hong

supporting information; experimental part, p. 224 - 226 (2011/03/19)

A novel class of primary amine-metal Lewis acid bifunctional catalysts based on a bidentate ligand was developed. These catalysts were highly efficient in catalyzing the direct asymmetric aldol reactions of ketones offering excellent stereoselectivity. Th

Synthesis of Pyridine Derivatives of L-Phenylalanine as Antisickling Reagents

Altman, Janina,Gorecki, Marian,Wilchek, Meir,Votano, Joseph R.,Rich, Alexander

, p. 596 - 600 (2007/10/02)

Several bicyclic agents composed of L-phenylalanine coupled to various pyridines were synthesized: 2-, 3-, and 4-(L-phenylalanylamino)pyridine.All three compounds at 3 mM gave positive morphological antisickling effects on homozygous SS cells under reduce

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