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1-(1-methylethyl)-10H-phenothiazine, also known as 1-isopropyl-10H-phenothiazine, is a chemical compound belonging to the phenothiazine family. It is characterized by a phenothiazine core, which consists of a tricyclic structure with a sulfur atom and a nitrogen atom in the central ring. The compound has an isopropyl group (1-methylethyl) attached to the nitrogen atom, which differentiates it from other phenothiazine derivatives. This chemical is primarily used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, such as tranquilizers, antihistamines, and insecticides. Due to its versatile structure, 1-(1-methylethyl)-10H-phenothiazine has potential applications in the development of new therapeutic agents and chemical products.

7240-76-8

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7240-76-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7240-76-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,4 and 0 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7240-76:
(6*7)+(5*2)+(4*4)+(3*0)+(2*7)+(1*6)=88
88 % 10 = 8
So 7240-76-8 is a valid CAS Registry Number.

7240-76-8SDS

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 1-propan-2-yl-10H-phenothiazine

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:7240-76-8 SDS

7240-76-8Downstream Products

7240-76-8Relevant academic research and scientific papers

THE TOTAL SYNTHESIS OF (+-)-C-MAVACURINE

Calverley, M. J.,Banks, B. J.,Harley-Mason, J.

, p. 1635 - 1638 (2007/10/02)

The processes of reductive opening and oxidative reclosing of the 3,4-bond have been applied to effect overall epimerisation at C-3 in the transformation of synthetic epi-geissoschizine analogues into mavacurine-type alkaloids.

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