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158144-84-4

3,5-BIS(TRIFLUOROMETHYL)BENZYL MERCAPTAN, with the molecular formula C9H5F6S, is a colorless to pale yellow liquid chemical compound. Characterized by two trifluoromethyl groups attached to a benzyl mercaptan moiety, it serves as a synthetic intermediate and reagent in organic synthesis. 3,5-BIS(TRIFLUOROMETHYL)BENZYL MERCAPTAN is also recognized for its strong odor, making it a component in perfumes and fragrances. Due to its toxic and irritating properties, it requires careful handling and adherence to safety protocols.

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  • 158144-84-4 Structure

  • Basic information

    1. Product Name: 3,5-BIS(TRIFLUOROMETHYL)BENZYL MERCAPTAN
    2. Synonyms: 3,5-BIS(TRIFLUOROMETHYL)BENZYL MERCAPTAN
    3. CAS NO:158144-84-4
    4. Molecular Formula: C9H6F6S
    5. Molecular Weight: 260.2
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 158144-84-4.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 3,5-BIS(TRIFLUOROMETHYL)BENZYL MERCAPTAN(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3,5-BIS(TRIFLUOROMETHYL)BENZYL MERCAPTAN(158144-84-4)
    11. EPA Substance Registry System: 3,5-BIS(TRIFLUOROMETHYL)BENZYL MERCAPTAN(158144-84-4)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 158144-84-4(Hazardous Substances Data)

158144-84-4 Usage

Uses

Used in Pharmaceutical Synthesis:
3,5-BIS(TRIFLUOROMETHYL)BENZYL MERCAPTAN is used as a building block for the synthesis of various pharmaceuticals. Its unique structure contributes to the development of new drugs with potential therapeutic applications.
Used in Agrochemical Production:
In the agrochemical industry, 3,5-BIS(TRIFLUOROMETHYL)BENZYL MERCAPTAN is utilized as a key intermediate in the creation of compounds designed to protect crops and enhance agricultural productivity.
Used in Material Science:
3,5-BIS(TRIFLUOROMETHYL)BENZYL MERCAPTAN is employed as a component in the synthesis of advanced materials, leveraging its chemical properties to improve material performance in various applications.
Used in Perfumery and Fragrance Industry:
Capitalizing on its strong odor, 3,5-BIS(TRIFLUOROMETHYL)BENZYL MERCAPTAN is used as a scent in perfumes and fragrances, adding depth and complexity to the olfactory profiles of these products.

Check Digit Verification of cas no

The CAS Registry Mumber 158144-84-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,8,1,4 and 4 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 158144-84:
(8*1)+(7*5)+(6*8)+(5*1)+(4*4)+(3*4)+(2*8)+(1*4)=144
144 % 10 = 4
So 158144-84-4 is a valid CAS Registry Number.

158144-84-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name [3,5-Bis(trifluoromethyl)phenyl]methanethiol

1.2 Other means of identification

Product number -
Other names 3,5-Bis(trifluoromethyl)benzyl mercaptan

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:158144-84-4 SDS

158144-84-4Relevant articles and documents

4-aminomethyl/thiomethyl/sulfonylmethyl-4-phenylpiperdines as tachykinin receptor antagonists

-

, (2008/06/13)

The present invention is directed to compounds of the formula (I) STR1 wherein R1, R2, R3, R5, R6, R7, R8, m, n and X are defined herein, and pharmaceutically acceptable salts th

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