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857244-78-1

thiotrithiazyl chloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 857244-78-1 Structure

  • Basic information

    1. Product Name: thiotrithiazyl chloride
    2. Synonyms: thiotrithiazyl chloride
    3. CAS NO:857244-78-1
    4. Molecular Formula:
    5. Molecular Weight: 205.737
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 857244-78-1.mol

  • 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: thiotrithiazyl chloride(CAS DataBase Reference)
    10. NIST Chemistry Reference: thiotrithiazyl chloride(857244-78-1)
    11. EPA Substance Registry System: thiotrithiazyl chloride(857244-78-1)

  • 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: 857244-78-1(Hazardous Substances Data)

857244-78-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 857244-78-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,7,2,4 and 4 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 857244-78:
(8*8)+(7*5)+(6*7)+(5*2)+(4*4)+(3*4)+(2*7)+(1*8)=201
201 % 10 = 1
So 857244-78-1 is a valid CAS Registry Number.

857244-78-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name thiotrithiazyl chloride

1.2 Other means of identification

Product number -
Other names -

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:857244-78-1 SDS

857244-78-1Relevant articles and documents

Reactions of the trisulfur trinitride anion, S3N3-, with halogens and other electrophilic substrates

Chivers, Tristram,Rao, M. N. Shudheendra

, p. 1957 - 1962 (2007/10/02)

The reactions of the trisulfur trinitride anion, S3N3-, with halogens (Cl2, Br2, I2), AsF5, SOCl2, SO2Cl2, S2Cl2, COCl2, CS2, Me3SiCl, and Ph2PCl have been investigated.In all cases these reactions gave mixtures of known sulfur-nitrogen compounds.Thus the halogens react with S3N3- to give mainly S4N4, S4N3+X- (X=Br, Cl), (SN)x, and S3N3X3 (X=Cl), while AsF5 oxidizes S3N3- to S4N4*AsF5.The major products of the reaction of S3N3- with SOCl2 or SO2Cl2 were S4N4, S4N3+Cl-, and (for SOCl2 only) S3N2O2.S3N2Cl was the main product of the reaction of S3N3- with S2Cl2, whereas COCl2 yielded (SN)x in addition to S3N2Cl and S4N4.Carbon disulfide reacts with S3N3- to give S4N2, S4N4, and CNS-.The cyclophosphathiazenes, (Ph2PN)(SN)2, 1,3- and 1,5-(Ph2PN)2(SN)2, in addition to (Ph2PN)x (x=3, 4), (Ph2PN)3*HCl and (Ph2PN)2NSCl were isolated from the reactions of Ph2PCl with S3N3- in various molar ratios.The latter reaction represents a useful alternative synthesis of the 1,5-isomer of the eight-membered ring (Ph2PN)2(SN)2.

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