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348-84-5

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348-84-5 Usage

Synonyms

4'-Chloro-3-trifluoromethylphenyl ethanol

Molecular weight

210.61 g/mol

Physical state

White crystalline solid

Uses

a. Synthesis of pharmaceuticals and agrochemicals
b. Starting material for various fine chemicals

Applications

a. Medicinal chemistry
b. Drug discovery

Pharmacological activity

Potential applications due to its pharmacological properties

Safety precautions

Handle with caution as it may pose risks to human health and the environment

Check Digit Verification of cas no

The CAS Registry Mumber 348-84-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,4 and 8 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 348-84:
(5*3)+(4*4)+(3*8)+(2*8)+(1*4)=75
75 % 10 = 5
So 348-84-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H8ClF3O/c1-5(14)6-2-3-8(10)7(4-6)9(11,12)13/h2-5,14H,1H3

348-84-5SDS

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 1-[4-chloro-3-(trifluoromethyl)phenyl]ethanol

1.2 Other means of identification

Product number -
Other names 1-[4-Chloro-3-(trifluoromethyl)phenyl]ethan-1-ol

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:348-84-5 SDS

348-84-5Relevant articles and documents

DERIVATIVES OF BENZOTHIAZINES, PREPARATION THEREOF AND APPLICATION THEREOF AS DRUGS

-

Page/Page column 102, (2010/09/18)

The object of the present invention is benzothiazine derivatives having the capability of inhibiting 11β-HSD1 not only at an enzymatic level but also at a cell level. The compounds of the present invention are of general formula (I). Wherein notably R1 represents a hydrogen or OR1 represents an ester or an ether. R2 represents a naphthyl or a 1, 2, 3, 4-tetrahydro-naphthalene or a biphenyl or phenyl pyridine or a substituted phenyl. R3 represents a methyl or ethyl; R4 and R'4 represent a hydrogen.

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