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27410-44-2

Benzothiazole, 2-[(1-methylethyl)thio]- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 27410-44-2 Structure

  • Basic information

    1. Product Name: Benzothiazole, 2-[(1-methylethyl)thio]- (9CI)
    2. Synonyms: Benzothiazole, 2-[(1-methylethyl)thio]- (9CI)
    3. CAS NO:27410-44-2
    4. Molecular Formula: C10H11NS2
    5. Molecular Weight: 209.33104
    6. EINECS: N/A
    7. Product Categories: BENZOTHIAZOLE
    8. Mol File: 27410-44-2.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 110-112 °C(Press: 0.5 Torr)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.22±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 0.90±0.10(Predicted)
    10. CAS DataBase Reference: Benzothiazole, 2-[(1-methylethyl)thio]- (9CI)(CAS DataBase Reference)
    11. NIST Chemistry Reference: Benzothiazole, 2-[(1-methylethyl)thio]- (9CI)(27410-44-2)
    12. EPA Substance Registry System: Benzothiazole, 2-[(1-methylethyl)thio]- (9CI)(27410-44-2)

  • 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: 27410-44-2(Hazardous Substances Data)

27410-44-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 27410-44-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,4,1 and 0 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 27410-44:
(7*2)+(6*7)+(5*4)+(4*1)+(3*0)+(2*4)+(1*4)=92
92 % 10 = 2
So 27410-44-2 is a valid CAS Registry Number.

27410-44-2SDS

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 2-(i-propylthio)benzo[d]thiazole

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:27410-44-2 SDS

27410-44-2Relevant articles and documents

ON THE REACTION OF BENZOTHIAZOL-2-YL SULPHENAMIDES WITH PHOSPHITES

Brownbridge, P.,Jowett, I. C.

, p. 311 - 318 (2007/10/02)

A study of the synthesis of phosphoramidates from phosphites and benzothiazol-2-yl-sulphenamides, indicates that a quinquecovalent phosphorane is an intermediate.Since the initial step in this reaction does not involve attack of phosphorus on nitrogen, it is unlikely that these sulphenamides will act as electrophilic aminating agents towards non-phosphorus nucleophiles.An efficient new method for preparing benzothiazol-2-yl-sulphenamides is reported.

REACTION OF SULFENAMIDES WITH DI-ALKYL AND TRIALKYL PHOSPHITES. AN EFFICIENT SYNTHESIS OF PHOSPHORAMIDATES BY UNUSUAL SUBSTITUTION AT S-N BOND IN (2-BENZOTHIAZOLYL)SULFENAMIDES

Torii, Sigeru,Sayo, Noboru,Tanaka, Hideo

, p. 695 - 698 (2007/10/02)

Regioselective attack of the trivalent phosphorus atom of dialkyl and trialkyl phosphites on either nitrogen or sulfur atom of sulfenamides has been found.The reaction of phenylsulfenamides with dialkyl phosphites yielded phosphorothiolates, whereas the treatment of (2-benzothiazolyl)sulfenamides with dialkyl and trialkyl phosphites gave phosphoramidates in excellent yields.

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