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CAS

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481697-67-0

Benzothiazole, 2-(3,3-dimethylbutyl)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 481697-67-0 Structure

  • Basic information

    1. Product Name: Benzothiazole, 2-(3,3-dimethylbutyl)- (9CI)
    2. Synonyms: Benzothiazole, 2-(3,3-dimethylbutyl)- (9CI)
    3. CAS NO:481697-67-0
    4. Molecular Formula: C13H17NS
    5. Molecular Weight: 219.34578
    6. EINECS: N/A
    7. Product Categories: BENZOTHIAZOLE
    8. Mol File: 481697-67-0.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: Benzothiazole, 2-(3,3-dimethylbutyl)- (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzothiazole, 2-(3,3-dimethylbutyl)- (9CI)(481697-67-0)
    11. EPA Substance Registry System: Benzothiazole, 2-(3,3-dimethylbutyl)- (9CI)(481697-67-0)

  • 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: 481697-67-0(Hazardous Substances Data)

481697-67-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 481697-67-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,8,1,6,9 and 7 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 481697-67:
(8*4)+(7*8)+(6*1)+(5*6)+(4*9)+(3*7)+(2*6)+(1*7)=200
200 % 10 = 0
So 481697-67-0 is a valid CAS Registry Number.

481697-67-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3,3-dimethylbutyl)-1,3-benzothiazole

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:481697-67-0 SDS

481697-67-0Downstream Products

481697-67-0Relevant articles and documents

Intermolecular coupling of alkenes to heterocycles via C-H bond activation

Tan, Kian L.,Park, Steve,Ellman, Jonathan A.,Bergman, Robert G.

, p. 7329 - 7335 (2004)

The intermolecular coupling of unactivated alkenes to a range of heterocycles using a Rh(I) catalyst was investigated. A variety of functional groups were incorporated into the alkene, including esters, nitriles, acetals, and phthalimide. Furthermore, the heterocycle tolerated substitution with both electron-rich and electron-deficient groups. The intermolecular coupling became possible after it was discovered that weak acids dramatically increase the rate of both the inter- and intramolecular reactions. An extensive optimization of additives was performed, and HCl·PCy3 (Cy = cyclohexyl) and HCl·P-t-Bu2Et were in general found to be the best additives for the reaction.

Intermolecular coupling of isomerizable alkenes to heterocycles via rhodium-catalyzed C-H bond activation

Tan, Kian L.,Bergman, Robert G.,Ellman, Jonathan A.

, p. 13964 - 13965 (2007/10/03)

This reports first intermolecular coupling of unactivated alkenes, including isomerizable alkenes, to a range of heterocycles using a Rh(I) catalyst. A variety of functional groups were incorporated, including esters, nitriles, and acetals. The intermolec

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