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Chlorsuperlutin is a synthetic chemical compound that has been used in the past for various purposes, including as a dye and in the production of certain pharmaceuticals. It is also known as 4-chloro-2,6-dimethylphenol, and it has a chemical formula of C8H9ClO. Due to its potential health risks and environmental concerns, the use of chlorsuperlutin has been restricted or banned in many countries. It is important to note that the compound should not be confused with chloramphenicol, an antibiotic with a similar name but different chemical properties and uses. Chlorsuperlutin's historical applications and current restrictions highlight the need for ongoing evaluation of chemical safety in various industries.

6799-23-1

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6799-23-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6799-23-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,9 and 9 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6799-23:
(6*6)+(5*7)+(4*9)+(3*9)+(2*2)+(1*3)=141
141 % 10 = 1
So 6799-23-1 is a valid CAS Registry Number.
InChI:InChI=1/C24H29ClO4/c1-13-10-19-17-12-21(25)20-11-16(28)6-8-22(20,4)18(17)7-9-23(19,5)24(13,14(2)26)29-15(3)27/h11-12,17-19H,1,6-10H2,2-5H3/t17-,18+,19+,22-,23+,24+/m1/s1

6799-23-1SDS

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 [(8R,9S,10R,13S,14S,17R)-17-acetyl-6-chloro-10,13-dimethyl-16-methylidene-3-oxo-1,2,8,9,11,12,14,15-octahydrocyclopenta[a]phenanthren-17-yl] acetate

1.2 Other means of identification

Product number -
Other names 17-Acetoxy-6-chloro-16-methylene-4,6-pregnadiene-3,20-dione

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:6799-23-1 SDS

6799-23-1Downstream Products

6799-23-1Relevant academic research and scientific papers

Synthesis and biological activity of 17-esters of 6-dehydro-16-methylene-17 -hydroxyprogesterones.

Shapiro,Weber,Harris,Miskowicz,Neri,Herzog

, p. 716 - 720 (1972)

Synthesis and biological activity of 17-esters of 6-dehydro-16-methylene-17 alpha-hydroxyprogesterone are presented. A systematic study of the influence of the alteration of halogen at 6 and the acyl group at 17 on the progestational and antiandrogenic activities of the resulting structures is described. A convenient general method for synthesis of all of the members of the generic family from the precursors in common is described. It is believed that 6-chloro-16-methylene-17 alpha-hydroxy-4,6-pregnadiene 17-acetate, because of its structural similarity to chlormadinone acetate and its high progestational potency, will perform as a contraceptive at perhaps a lower dose than that of chlormadinone acetate.

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