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Acetic acid, (1,1-dimethylethoxy)-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

137676-99-4

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137676-99-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 137676-99-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,6,7 and 6 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 137676-99:
(8*1)+(7*3)+(6*7)+(5*6)+(4*7)+(3*6)+(2*9)+(1*9)=174
174 % 10 = 4
So 137676-99-4 is a valid CAS Registry Number.

137676-99-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(1,1-dimethylethoxy)acetic acid methyl ester

1.2 Other means of identification

Product number -
Other names tert-Butoxy-acetic acid methyl 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:137676-99-4 SDS

137676-99-4Downstream Products

137676-99-4Relevant academic research and scientific papers

Lewis base activation of Lewis acids: Catalytic, enantioselective addition of glycolate-derived silyl ketene acetals to aldehydes

Denmark, Scott E.,Chung, Won-Jin

, p. 4582 - 4595 (2008/09/21)

(Chemical Equation Presented) A catalytic system involving silicon tetrachloride and a chiral, Lewis basic bisphosphoramide catalyst is effective for the addition of glycolate-derived silyl ketene acetals to aldehydes. It was found that the sense of diast

Evaluation of copper chelation agents as anti-angiogenic therapy

Camphausen, Kevin,Sproull, Mary,Tantama, Steve,Sankineni, Sandeep,Scott, Tamalee,Menard, Cynthia,Coleman, C.Norman,Brechbiel, Martin W.

, p. 4287 - 4293 (2007/10/03)

The design, synthesis and evaluation of N,N′,N″-tris(2-pyridylmethyl)-cis,cis-1,3,5,-triaminocyclohexane (tachpyr, 1) derivatives as novel anti-angiogenic agents were performed in an in vitro endothelial cell proliferation assay to assess their cytotoxicity and selectivity. The selective nature of the anti-angiogenic agents for human umbilical vein endothelial cells (Huvec) was compared to a normal fibroblast cell line and a human Glioma cell line to evaluate these compounds. N,N′,N″-tris(2-mercaptoethyl)-cis,cis-1,3,5-triaminocyclohexane trihydrochloride (3b) was superior to tachpyr in terms of selectivity of its inhibitory activity toward the proliferation of Huvec compared to the fibroblast and human Glioma cell lines.

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