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5-AMino-2-pyridineacetic acid Methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

174891-11-3

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174891-11-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 174891-11-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,4,8,9 and 1 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 174891-11:
(8*1)+(7*7)+(6*4)+(5*8)+(4*9)+(3*1)+(2*1)+(1*1)=163
163 % 10 = 3
So 174891-11-3 is a valid CAS Registry Number.

174891-11-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl (5-amino-2-pyridinyl)acetate

1.2 Other means of identification

Product number -
Other names -

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:174891-11-3 SDS

174891-11-3Downstream Products

174891-11-3Relevant academic research and scientific papers

External-Photocatalyst-Free Visible-Light-Mediated Synthesis of Indolizines

Sahoo, Basudev,Hopkinson, Matthew N.,Glorius, Frank

, p. 15545 - 15549 (2016/01/26)

A visible-light-mediated synthesis of valuable polycyclic indolizine heterocycles from easily accessed brominated pyridine and enol carbamate derivatives has been developed. This process, which operates at room temperature under irradiation from readily available light sources, does not require the addition of an external photocatalyst. Instead, an investigation into the reaction mechanism indicates that the indolizine products themselves may be in some way involved in mediating and accelerating their own formation. Preliminary studies also show that these simple heterocyclic compounds may be capable of facilitating other visible-light-mediated transformations.

COMPOUNDS AND THEIR METHODS OF USE

-

, (2014/05/25)

Compounds and compositions comprising compounds that inhibit glutaminase are described herein. Also described herein are methods of using the compounds that inhibit glutaminase in the treatment of cancer.

COMPOUNDS, PHARMACEUTICAL COMPOSITIONS AND USES AS GLUTAMINASE INHIBITORS FOR TREATING CANCERS THEREOF

-

, (2014/06/11)

Provided are compounds of formula (I), wherein X, Y, Z, W, m, n, o, p, R1, R2 and R6 are defined as in the description. Pharmaceutical compositions and uses as glutaminase inhibitors for treating cancers thereof are also provided.

COMPOUNDS AND THEIR METHODS OF USE

-

, (2014/06/11)

Provided are compounds of formula (I), which can inhibit glutaminase. Pharmaceutical compositions comprising these compounds and uses as glutaminase inhibitors for treating cancers thereof are also provided.

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