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methyl 3-(acetoxymethyl)-4-bromobenzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

254746-41-3

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254746-41-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 254746-41-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,4,7,4 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 254746-41:
(8*2)+(7*5)+(6*4)+(5*7)+(4*4)+(3*6)+(2*4)+(1*1)=153
153 % 10 = 3
So 254746-41-3 is a valid CAS Registry Number.

254746-41-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 3-(acetyloxymethyl)-4-bromobenzoate

1.2 Other means of identification

Product number -
Other names methyl 3-(acetoxymethyl)-4-bromobenzoate

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:254746-41-3 SDS

254746-41-3Relevant academic research and scientific papers

OXADIAZOLE FUSED HETEROCYCLIC DERIVATIVES USEFUL FOR THE TREATMENT OF MULTIPLE SCLEROSIS

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Page/Page column 61-62, (2010/08/05)

The invention provides compounds of Formula (I) for the treatment of multiple sclerosis and other diseases.

BIS-(SULFONYLAMINO) DERIVATIVES FOR TREATMENT OF PAIN AND INFLAMMATION

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Page/Page column 74, (2010/12/17)

The invention provides compounds of formula (I) wherein R1, R2, R3, A and m are as defined in the specification and optical isomers, racemates and tautomers thereof, and pharmaceutically acceptable salts thereof; together

BIS-(SULFONYLAMINO) DERIVATIVES IN THERAPY 065

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Page/Page column 51-52, (2009/05/28)

The invention provides compounds of formula wherein R1, R2, R3, A and m are as defined in the specification and optical isomers, racemates and tautomers thereof, and pharmaceutically acceptable salts thereof; together with processes for their preparation, pharmaceutical compositions containing them and their use in therapy. The compounds are inhibitors of microsomal prostaglandin E synthase-1

OXADIAZOLE DIARYL COMPOUNDS

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Page/Page column 12; 77, (2009/05/29)

The invention relates to compounds of formula (I): wherein R1, R2, Ra , Rb,Rc and W, have the meanings given in claim 1. The compounds are useful e.g. in the treatment of autoimmune disorders, such as multiple sclerosis.

BIS-(SULFONYLAMINO) DERIVATIVES IN THERAPY 066

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Page/Page column 104, (2009/06/27)

The invention provides compounds of formula wherein R1, R3, L1, L2, G1, G2, A and m are as defined in the specification and optical isomers, racemates and tautomers thereof, and pharmaceutically acceptable salts thereof; together with processes for their preparation, pharmaceutical compositions containing them and their use in therapy. The compounds are inhibitors of microsomal prostaglandin E synthase-1.

Potent and selective TF/FVIIa inhibitors containing a neutral P1 ligand

Miura, Masanori,Seki, Norio,Koike, Takanori,Ishihara, Tsukasa,Niimi, Tatsuya,Hirayama, Fukushi,Shigenaga, Takeshi,Sakai-Moritani, Yumiko,Kawasaki, Tomihisa,Sakamoto, Shuichi,Okada, Minoru,Ohta, Mitsuaki,Tsukamoto, Shin-ichi

, p. 7688 - 7705 (2007/10/03)

Inhibition of tissue factor/factor VIIa complex (TF/FVIIa) is an attractive strategy for antithrombotic therapies. We began with an investigation of a non-amidine TF/FVIIa inhibitor based on a modification of amidine compound 1. Optimization of the substituents on the P1 phenyl portion of the compound 1 led to a neutral or less basic alternative for the 4-amidinophenyl moiety. By further optimization of the substituents on the central phenyl ring, a highly potent and selective TF/FVIIa inhibitor 17d was discovered.

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