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9H-Thioxanthene-3-carbonylchloride, 9-oxo-, 10,10-dioxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

97404-16-5

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97404-16-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 97404-16-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,4,0 and 4 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 97404-16:
(7*9)+(6*7)+(5*4)+(4*0)+(3*4)+(2*1)+(1*6)=145
145 % 10 = 5
So 97404-16-5 is a valid CAS Registry Number.

97404-16-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 9,10,10-trioxothioxanthene-3-carbonyl chloride

1.2 Other means of identification

Product number -
Other names EINECS 306-779-6

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:97404-16-5 SDS

97404-16-5Downstream Products

97404-16-5Relevant academic research and scientific papers

Articles Comprising Benzopyran Colorants, Method Of Manufacture, And Method Of Use

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Page/Page column 7, (2008/06/13)

An article comprising the compound of Formula (I) wherein X is hydrogen or a radical of Formula (II), R1 independently at each occurrence is a C1-C20 aliphatic radical, a C3-C10 cycloaliphatic radical, or a C3-C10 aromatic radical; R2, R3, R4 and R5 are independently at each occurrence a halogen, a nitro group, a cyano group, a hydroxy group, a C1-C20 aliphatic radical, a C3-C20 cycloaliphatic radical, or a C6-C20 aromatic radical; and “n”, “q”, and “p” are each independently integers having a value of 0 to 3, and “m” is an integer having a value of 0 to 4.

Selective inhibitors of monoamine oxidase. 4. SAR of tricyclic N- methylcarboxamides and congeners binding at the tricyclics' hydrophilic binding site

Harfenist, Morton,Joseph, Diane M.,Spence, Sharon C.,Mcgee, Daniel P. C.,Reeves, Mark D.,White, Helen L.

, p. 2466 - 2473 (2007/10/03)

Linear [6.6.6] tricyclic moieties whose center ring is made of two atoms of differing size (here primarily thioxanth-9-ones and phenoxathiins) monosubstituted meta to the sulfur by C(O)NHMe include potent and selective inhibitors of monoamine oxidase A. Similarities with effects on SAR of acylamide and of diazapentacyclic substitution on such rings, including positional variables, the requirement for monomethylation (primary and dialkylated amides are inactive and higher monoalkylated amides show little or no potency), and that sulfur is optimally in sulfone form, suggest that binding to the enzyme occurs similarly in each series. No significantly greater rise in blood pressure was found in rats given sufficient 8 to inhibit most brain and liver MAO A and then followed by oral tyramine than was found on administration of tyramine to controls. This is in contrast to a large blood pressure rise in rats pretreated with phenelzine followed by tyramine, and in accord with the belief that an inhibitor selective for MAO A which is reversibly bound to the enzyme and therefore displaced by any ingested tyramine will not lead to the 'cheese effect' (hypertension during treatment with MAO inhibitors usually caused by ingestion of foods containing tyramine).

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