195006-26-9

• 

• Basic information

  1. Product Name: 1,3-Dithiole, 2-[4,5-bis[[[4-(chloromethyl)phenyl]methyl]thio]-1,3-dithiol-2-ylidene]-4,5- bis[[[4-(chloromethyl)phenyl]methyl]thio]-
  2. Synonyms:
  3. CAS NO:195006-26-9
  4. Molecular Formula: C38H32Cl4S8
  5. Molecular Weight: 887.012
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 195006-26-9.mol
  9. Article Data: 1

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: N/A
  3. Flash Point: N/A
  4. Appearance: N/A
  5. Density: N/A
  6. Refractive Index: N/A
  7. Storage Temp.: N/A
  8. Solubility: N/A
  9. CAS DataBase Reference: 1,3-Dithiole, 2-[4,5-bis[[[4-(chloromethyl)phenyl]methyl]thio]-1,3-dithiol-2-ylidene]-4,5- bis[[[4-(chloromethyl)phenyl]methyl]thio]-(CAS DataBase Reference)
  10. NIST Chemistry Reference: 1,3-Dithiole, 2-[4,5-bis[[[4-(chloromethyl)phenyl]methyl]thio]-1,3-dithiol-2-ylidene]-4,5- bis[[[4-(chloromethyl)phenyl]methyl]thio]-(195006-26-9)
  11. EPA Substance Registry System: 1,3-Dithiole, 2-[4,5-bis[[[4-(chloromethyl)phenyl]methyl]thio]-1,3-dithiol-2-ylidene]-4,5- bis[[[4-(chloromethyl)phenyl]methyl]thio]-(195006-26-9)

• 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: 195006-26-9(Hazardous Substances Data)

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• 1,3-Dithiole, 2-[4,5-bis[[[4-(chloromethyl)phenyl]methyl]thio]-1,3-dithiol-2-ylidene]-4,5- bis[[[4-(chloromethyl)phenyl]methyl]thio]-

  Cas No: 195006-26-9

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195006-26-9 Usage

Chemical structure

The compound has a dithiole core with two 1,3-dithiole rings and is substituted with chloromethylphenyl groups on both rings.

Sulfur-containing molecule

The compound contains sulfur atoms in its structure, which may contribute to its reactivity and interactions with biological systems.

Chloromethylphenyl groups

The compound has multiple chloromethylphenyl groups attached to the dithiole rings, which may affect its reactivity and potential applications.

Potential reactivity

The complex structure of the compound suggests that it may have reactivity and complex interactions with biological systems.

Applications

The compound may have potential applications in various fields, including medicine, materials science, and organic synthesis.

Handling and study

Due to its complex structure and potential reactivity, the compound should be handled and studied with care.

Research focus

Further research is needed to fully understand the properties, reactivity, and potential applications of this complex compound.

Check Digit Verification of cas no

The CAS Registry Mumber 195006-26-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,5,0,0 and 6 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 195006-26:
(8*1)+(7*9)+(6*5)+(5*0)+(4*0)+(3*6)+(2*2)+(1*6)=129
129 % 10 = 9
So 195006-26-9 is a valid CAS Registry Number.

195006-26-9SDS

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	tetrakis(4-chlormethylbenzylthio)tetrathiafulvalene

1.2 Other means of identification

Product number	-
Other names	4,5,4',5'-Tetrakis-(4-chloromethyl-benzylsulfanyl)-[2,2']bi[[1,3]dithiolylidene]

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:195006-26-9 SDS

195006-26-9Upstream product

• 195006-24-7 4,5-bis(4-chloromethylbenzylthio)-1,3-dithiole-2-thione 
• 623-25-6 p-Xylylene dichloride 
• 195006-25-8 4,5-bis(4-chloromethylbenzylthio)-1,3-dithiole-2-one 

195006-26-9Downstream Products

195006-26-9Relevant articles and documents

Synthesis and electrochemistry of new tetrathiafulvalene (TTF) dendrimers: X-ray crystal structure of a tetrafunctionalised TTF core unit

Wang, Changsheng

, p. 1189 - 1197 (2007/10/03)

A new synthetic approach to tetrathiafulvalene (TTF) dendrimers is reported. Tetrakis(4-chloromethylbenzylthio)tetra-thiafulvalene 7 is a functionalised core unit which reacts with four equivalents of the thiolate ion generated from compound 16 to afford

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