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3065-79-0

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3065-79-0 Usage

Chemical Properties

brown powder

Uses

3,3′-Diethyl-9-methylthiacarbocyanine iodide a stain used for research purposes.

Check Digit Verification of cas no

The CAS Registry Mumber 3065-79-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,6 and 5 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3065-79:
(6*3)+(5*0)+(4*6)+(3*5)+(2*7)+(1*9)=80
80 % 10 = 0
So 3065-79-0 is a valid CAS Registry Number.

3065-79-0 Well-known Company Product Price

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  • (Code)Product description
  • CAS number
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  • Detail
  • Alfa Aesar

  • (H55144)  3,3'-Diethyl-9-methylthiacarbocyanine iodide, 98%   

  • 3065-79-0

  • 250mg

  • 750.0CNY

  • Detail
  • Alfa Aesar

  • (H55144)  3,3'-Diethyl-9-methylthiacarbocyanine iodide, 98%   

  • 3065-79-0

  • 1g

  • 2402.0CNY

  • Detail

3065-79-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (2Z)-3-ethyl-2-[(E)-3-(3-ethyl-1,3-benzothiazol-3-ium-2-yl)-2-methylprop-2-enylidene]-1,3-benzothiazole,iodide

1.2 Other means of identification

Product number -
Other names Benzothiazolium,3-ethyl-2-(3-(3-ethyl-2-benzothiazolinylidene)-2-methyl-1-propenyl)-,iodide

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:3065-79-0 SDS

3065-79-0Relevant articles and documents

CONDENSATION OF VILSMEIER COMPLEXES WITH HETEROCYCLIC COMPOUNDS. SYNTHESIS OF CARBOCYANINES

Makin, S. M.,Pomogaev, A. I.

, p. 1916 - 1918 (2007/10/02)

Carbocyanine dyes are formed in the reaction of the quaternary salts of heterocyclic bases containing an active methyl group with the complexes of carboxamides and phosphorus oxychloride.A series of carbocyanines were synthesized, including those containing various substituents at the meso position of the trimethine chain.

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