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918328-15-1

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918328-15-1 Usage

Molecular Weight

217.12 g/mol

Physical State

Colorless to light yellow liquid

Odor

Strong, sweet odor

Primary Use

Intermediate in pharmaceutical and organic compound synthesis

Secondary Use

Reagent in chemical research and manufacturing

Handling Precautions

May cause irritation to skin, eyes, and respiratory system
Harmful if ingested or inhaled

Check Digit Verification of cas no

The CAS Registry Mumber 918328-15-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,8,3,2 and 8 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 918328-15:
(8*9)+(7*1)+(6*8)+(5*3)+(4*2)+(3*8)+(2*1)+(1*5)=181
181 % 10 = 1
So 918328-15-1 is a valid CAS Registry Number.

918328-15-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-bromo-2-methylsulfanylphenyl)methanol

1.2 Other means of identification

Product number -
Other names Benzenemethanol,4-bromo-2-(methylthio)

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:918328-15-1 SDS

918328-15-1Downstream Products

918328-15-1Relevant articles and documents

PYRIMIDINE DERIVATIVES AS PGE2 RECEPTOR MODULATORS

-

, (2018/12/13)

The present invention relates to pyrimidine derivatives of formula (I) wherein (R1)n, R3, R4a, R4b, R5a, R5b and Ar1 are as described in the description and their use in the treatment of cancer by modulating an immune response comprising a reactivation of the immune system in the tumor. The invention further relates to novel benzofurane and benzothiophene derivatives of formula (II) and their use as pharmaceuticals, to their preparation, to pharmaceutically acceptable salts thereof, and to their use as pharmaceuticals, to pharmaceutical compositions containing one or more compounds of formula (I), and especially to their use as modulators of the prostaglandin 2 receptors EP2 and/or EP4.

Discovery of Highly Potent Liver X Receptor β Agonists

Kick, Ellen K.,Busch, Brett B.,Martin, Richard,Stevens, William C.,Bollu, Venkataiah,Xie, Yinong,Boren, Brant C.,Nyman, Michael C.,Nanao, Max H.,Nguyen, Lam,Plonowski, Artur,Schulman, Ira G.,Yan, Grace,Zhang, Huiping,Hou, Xiaoping,Valente, Meriah N.,Narayanan, Rangaraj,Behnia, Kamelia,Rodrigues, A. David,Brock, Barry,Smalley, James,Cantor, Glenn H.,Lupisella, John,Sleph, Paul,Grimm, Denise,Ostrowski, Jacek,Wexler, Ruth R.,Kirchgessner, Todd,Mohan, Raju

supporting information, p. 1207 - 1212 (2016/12/18)

Introducing a uniquely substituted phenyl sulfone into a series of biphenyl imidazole liver X receptor (LXR) agonists afforded a dramatic potency improvement for induction of ATP binding cassette transporters, ABCA1 and ABCG1, in human whole blood. The ag

LIVER X RECEPTOR (LXR) MODULATORS

-

Page/Page column 111, (2015/03/28)

Described herein are liver X receptor (LXR) modulators and methods of utilizing LXR modulators in the treatment of dermal diseases, disorders or conditions. Also described herein are pharmaceutical compositions containing such compounds.

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