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6,8a-dimethyl-4,6,8,8a-tetrahydro-7H-[1,3]thiazolo[4,5-e]indol-7-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

79123-76-5

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79123-76-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79123-76-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,1,2 and 3 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 79123-76:
(7*7)+(6*9)+(5*1)+(4*2)+(3*3)+(2*7)+(1*6)=145
145 % 10 = 5
So 79123-76-5 is a valid CAS Registry Number.

79123-76-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 6,8a-dimethyl-4,8-dihydropyrrolo[3,2-e][1,3]benzothiazol-7-one

1.2 Other means of identification

Product number -
Other names 6,8a-Dimethyl-4,6,8,8a-tetrahydro-7H-(1,3)thiazolo(4,5-e)indol-7-one

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:79123-76-5 SDS

79123-76-5Downstream Products

79123-76-5Relevant academic research and scientific papers

Thiazole analogs of benzomorphans. I. Synthesis of novel thiazolo[4,5-f]morphans

Katsuura,Ohta,Mitsuhashi

, p. 4378 - 4383 (1982)

The synthesis and analgesic properties of thiazolo[4,5-f]morphans (XIIa-c) are described. Monothiazolization of ethyl 2-methyl-1,3-dioxo-2-cyclohexaneacetate (I) afforded the 2-aminothiazole derivative (II), which was deaminated to ethyl 4,5,6,7-tetrahydro-4-methyl-5-oxo-4-benzothiazoleacetate (V) by means of the Sandmeyer reaction and subsequent hydrogenolysis of the resulting chloride (IVa). In several steps, V was converted to 2,5-dimethyl-9-oxothiazolo[4,5-f]morphan (X). Thiazolo[4,5-f]morphan derivatives (XIIa-c) were synthesized from this key intermediate (X).

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