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1236-00-6

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1236-00-6 Usage

Uses

10β-Hydroxynorethindrone is the 6β-hydroxy analogue and a by-product of Norethindrone (N676000) synthesis. 10β-Hydroxynorethindrone is also a metabolite of the progestagen hormone, Lynestrenol.

Check Digit Verification of cas no

The CAS Registry Mumber 1236-00-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,3 and 6 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1236-00:
(6*1)+(5*2)+(4*3)+(3*6)+(2*0)+(1*0)=46
46 % 10 = 6
So 1236-00-6 is a valid CAS Registry Number.
InChI:InChI=1/C20H26O3/c1-3-19(22)10-8-16-15-5-4-13-12-14(21)6-11-20(13,23)17(15)7-9-18(16,19)2/h1,12,15-17,22-23H,4-11H2,2H3/t15-,16-,17-,18-,19-,20+/m0/s1

1236-00-6SDS

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 10β-Hydroxy Norethindrone

1.2 Other means of identification

Product number -
Other names (8S,9S,10S,13S,14S,17R)-17-ethynyl-10,17-dihydroxy-13-methyl-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-3-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:1236-00-6 SDS

1236-00-6Downstream Products

1236-00-6Relevant articles and documents

Oxidation of lynestrenol by the fungus Cunninghamella elegans

Iqbal Choudhary,Atif

experimental part, p. 1 - 6 (2010/04/23)

Transformation of lynestrenol (19-nor-17α-pregn-4-en-20-yn-17β- ol) (1) was carried out by incubation with Cunninghamella elegans to obtain 19-nor-17α-pregn-4-en-20-yn-3-one-10β,17β-diol (2), 19-nor-17α-pregn-4-en-20-yn-3-one-6β,17β-diol (3), and 19-nor-17α-pregn-4-en-20-yn-3β,6β,17β-triol (4). Metabolite 4 was identified as a new compound. These metabolites were structurally characterised on the basis of spectroscopic techniques.

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