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36480-40-7

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  • 36480-40-7 Structure

  • Basic information

    1. Product Name: 3,4-DICHLOROBENZYL MERCAPTAN
    2. Synonyms: 3,4-DICHLOROBENZENEMETHANETHIOL;3,4-DICHLOROBENZYL MERCAPTAN;(3,4-Dichlorophenyl)methanethiol;Benzenemethanethiol, 3,4-dichloro-;3,4-dichlorotoluene-alpha-thiol;3,4-Dichloro-alpha-toluenethiol;3,4-dichloro-à-toluenethiol
    3. CAS NO:36480-40-7
    4. Molecular Formula: C7H6Cl2S
    5. Molecular Weight: 193.09
    6. EINECS: 253-054-4
    7. Product Categories: N/A
    8. Mol File: 36480-40-7.mol
    9. Article Data: 3

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 152-153°C 12mm
    3. Flash Point: 152-153°C/12mm
    4. Appearance: /
    5. Density: 1.362
    6. Vapor Pressure: 0.0121mmHg at 25°C
    7. Refractive Index: 1.6080
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. PKA: 8.83±0.10(Predicted)
    11. Water Solubility: Difficult to mix in water.
    12. Sensitive: Air Sensitive
    13. BRN: 3237473
    14. CAS DataBase Reference: 3,4-DICHLOROBENZYL MERCAPTAN(CAS DataBase Reference)
    15. NIST Chemistry Reference: 3,4-DICHLOROBENZYL MERCAPTAN(36480-40-7)
    16. EPA Substance Registry System: 3,4-DICHLOROBENZYL MERCAPTAN(36480-40-7)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: 20/21/22
    3. Safety Statements: 23-36/37
    4. RIDADR: 2810
    5. WGK Germany:
    6. RTECS:
    7. HazardClass: 6.1
    8. PackingGroup: III
    9. Hazardous Substances Data: 36480-40-7(Hazardous Substances Data)

36480-40-7 Usage

Description

3,4-Dichlorobenzyl Mercaptan is an organic compound characterized by the presence of a sulfur atom bonded to a benzene ring with two chlorine atoms at the 3rd and 4th positions. It is known for its unique chemical properties and potential applications in various industries.

Uses

Used in Chemical Synthesis:
3,4-Dichlorobenzyl Mercaptan is used as a reagent in the synthesis of substituted pyridazines, which are important compounds in the pharmaceutical and chemical industries due to their diverse biological activities and potential applications as therapeutic agents.
Used in Semiconductor Industry:
3,4-Dichlorobenzyl Mercaptan is utilized as an additive to improve the morphologies of semiconductor materials. Its incorporation can enhance the performance and efficiency of semiconductor devices by optimizing their structural properties and electronic characteristics.

Check Digit Verification of cas no

The CAS Registry Mumber 36480-40-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,4,8 and 0 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 36480-40:
(7*3)+(6*6)+(5*4)+(4*8)+(3*0)+(2*4)+(1*0)=117
117 % 10 = 7
So 36480-40-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H6Cl2S/c8-6-2-1-5(4-10)3-7(6)9/h1-3,10H,4H2

36480-40-7 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail

  • Alfa Aesar

  • (L03226)  3,4-Dichlorobenzyl mercaptan, 97%   

  • 36480-40-7

  • 1g

  • 594.0CNY

  • Detail

  • Alfa Aesar

  • (L03226)  3,4-Dichlorobenzyl mercaptan, 97%   

  • 36480-40-7

  • 5g

  • 1991.0CNY

  • Detail

36480-40-7SDS

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 (3,4-dichlorophenyl)methanethiol

1.2 Other means of identification

Product number -
Other names 3,4-DICHLOROBENZYL 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:36480-40-7 SDS

36480-40-7Relevant articles and documents

Synthesis and Biological Activity of trans-(+/-)-N-Methyl-2-(3-pirydyl)-2-tetrahydrothiopyrancarbothioamide 1-Oxide (RP 49356) and Analogues: A New Class of Potassium Channel Opener

Brown, Thomas J.,Chapman, Robert F.,Cook, David C.,Hart, Terance W.,McLay, Iain M.,et al.

, p. 3613 - 3624 (2007/10/02)

The synthesis and biological activity of trans-(+/-)-N-methyl-2-(3-pyridyl)-2-tetrahydrothiopyrancarbothioamide 1-oxide (8a, RP 49356) and analoques is reported.These compounds constitute a new structural class of K+-channel opener.The effects of changes in the pyridyl group, thioamide, and thiane ring on in vitro K+-channel opening activity are discussed.A 3-pyridyl or 3-quinolyl group, a small N-alkyl thioamide function, and a thiane oxide ring, in which the sulfoxide is in a trans relationship to thioamide, are preferred for activity.Selected compounds were tested intravenously in the normotensive anaesthetized rat for hypotensive effects, and the activities reflect their in vitro K+-channel opening activity.This led to further evaluation of compound 8a and the selection of the (-)-enantiomer 8b (RP 52891) for development as an antihypertensive and antianginal agent.

Synthesis of certain derivatives of thiols.

BOENIGK,CHRISTIAN,JENKINS

, p. 357 - 360 (2007/10/06)

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