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butanoic acid,4-{(4-methoxyphenyl)methoxy}-3-oxo-,methyl este is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

921209-92-9

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921209-92-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 921209-92-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,1,2,0 and 9 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 921209-92:
(8*9)+(7*2)+(6*1)+(5*2)+(4*0)+(3*9)+(2*9)+(1*2)=149
149 % 10 = 9
So 921209-92-9 is a valid CAS Registry Number.

921209-92-9SDS

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 4-[(4-methoxyphenyl)methoxy]-3-oxobutanoate

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:921209-92-9 SDS

921209-92-9Downstream Products

921209-92-9Relevant articles and documents

Synthesis of the tricyclic core of 5α-capnellenols using asymmetric Heck reaction-carbanion capture process

Itano, Wataru,Ohshima, Takashi,Shibasaki, Masakatsu

, p. 3053 - 3056 (2008/02/13)

The tricyclic core of 5α-capnellenols was synthesized using an asymmetric Heck reaction-carbanion capture process and an intramolecular nitrile oxide cycloaddition as key ring construction steps. Moreover, the desired C5-α-OH product was obtained through

SUBSTITUTED 3-AMINO-THIENO[2,3-b]PYRIDINE-2-CARBOXYLIC ACID AMIDE COMPOUNDS AND PROCESSES FOR PREPARING AND THEIR USES

-

Page 127-130, (2008/06/13)

Disclosed are compounds of formula (I), wherein R1 and R2 are defined herein, which are useful as inhibitors of the kinase activity of the IκB kinase (IKK) complex. The compounds are therefore useful in the treatment of IKK mediated diseases including autoimmune diseases inflammatory diseases and cancer. Also disclosed are pharmaceutical compositions comprising these compounds and processes for preparing these compounds.

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