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Benzoic acid,2,4-diMethoxy-6-Methyl-,2- Methylpropyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1276019-92-1

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1276019-92-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1276019-92-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,7,6,0,1 and 9 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1276019-92:
(9*1)+(8*2)+(7*7)+(6*6)+(5*0)+(4*1)+(3*9)+(2*9)+(1*2)=161
161 % 10 = 1
So 1276019-92-1 is a valid CAS Registry Number.

1276019-92-1SDS

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 Benzoic acid, 2,4-dimethoxy-6-methyl-, 2-methylpropyl ester

1.2 Other means of identification

Product number -
Other names Benzoic acid, 2,4-dimethoxy-6-methyl-, 2-methylpropyl 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:1276019-92-1 SDS

1276019-92-1Relevant academic research and scientific papers

Synthesis, modification, and evaluation of (R)-de-O-methyllasiodiplodin and analogs as nonsteroidal antagonists of mineralocorticoid receptor

Jiang, Cheng-Shi,Zhou, Rong,Gong, Jing-Xu,Chen, Li-Li,Kurtán, Tibor,Shen, Xu,Guo, Yue-Wei

supporting information; experimental part, p. 1171 - 1175 (2011/04/16)

Macrolide (R)-de-O-methyllasiodiplodin (1), discovered to be a potent nonsteroidal antagonist of the mineralocorticoid receptor (MR), was synthesized via an efficient method and evaluated for MR antagonistic activity together with its analogs. Among all the tested compounds, compounds 18a, 18b and 18c, exhibited more potent antagonistic activity against MR with IC50 values ranging from 0.58 to 1.11 μM. Generally, it was obviously demonstrated that acetylation at phenolic hydroxyl groups and the ring size in analogs of 1 were very important for MR antagonist activity.

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