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38002-18-5

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38002-18-5 Usage

Uses

An oxidative tranformation product of Norethindrone Acetate (N675990) and Ethynyl Estradiol (E685100).

Check Digit Verification of cas no

The CAS Registry Mumber 38002-18-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,0,0 and 2 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 38002-18:
(7*3)+(6*8)+(5*0)+(4*0)+(3*2)+(2*1)+(1*8)=85
85 % 10 = 5
So 38002-18-5 is a valid CAS Registry Number.

38002-18-5 Well-known Company Product Price

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  • USP

  • (1260012)  Ethinyl estradiol Related Compound A  United States Pharmacopeia (USP) Reference Standard

  • 38002-18-5

  • 1260012-20MG

  • 14,578.20CNY

  • Detail

38002-18-5SDS

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 (8R,9S,13S,14S,17R)-17-ethynyl-3,17-dihydroxy-13-methyl-7,8,9,11,12,14,15,16-octahydrocyclopenta[a]phenanthren-6-one

1.2 Other means of identification

Product number -
Other names 6-oxo ethinylestradiol

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:38002-18-5 SDS

38002-18-5Relevant articles and documents

Synthesis and crystal structure of a new mestranol acetate

Li, Hongqi,Qian, Haichuan,Li, Jinxing,Ma, Shuwen

, p. 1208 - 1213 (2011)

A new mestranol acetate, 17α-ethinyl-17-hydroxy-3-methoxyestra-1,3, 5(10)-triene-6-one-17-acetate, was synthesized by an efficient three-step sequence starting from norethindrone. The structure of the new steroid was characterized by 1H NMR, 13C NMR, MS, IR spectrum and X-ray single crystal diffraction. It crystallizes in the triclinic system, space group P1. The molecules are arranged in a head-to-tail fashion without intra- and intermolecular hydrogen bonding.

A Novel Efficient Approach to the Synthesis of 6-Oxo Ethinylestradiol and its 3-Isopropanesulfonate

Weber, Gisela,Schaumann, J.,Carl, Constanze,Schwarz, S.,Leisner, Rosemarie

, p. 223 - 230 (2007/10/02)

Ethinylestradiol (1) was converted into the corresponding 6-oxo derivative 7 by a short and simple procedure involving acetate 10 and ketone 11.Phase transfer catalyzed esterification of compound 7 with propane-2-sulfonyl chloride gave sulfonate 12.

Thermal degradation of mestranol and ethinyl estradiol

Cotter,Levine,Mallory,Shaw

, p. 1939 - 1942 (2007/10/12)

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