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14009-70-2

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14009-70-2 Usage

Uses

Different sources of media describe the Uses of 14009-70-2 differently. You can refer to the following data:
1. Mestranol
2. Mestranol (M258755) derivative. It is used as contraceptive.

Check Digit Verification of cas no

The CAS Registry Mumber 14009-70-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,0,0 and 9 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 14009-70:
(7*1)+(6*4)+(5*0)+(4*0)+(3*9)+(2*7)+(1*0)=72
72 % 10 = 2
So 14009-70-2 is a valid CAS Registry Number.
InChI:InChI=1/C22H28O2/c1-4-21-12-10-18-17-9-7-16(24-3)14-15(17)6-8-19(18)20(21)11-13-22(21,23)5-2/h2,7,9,14,18-20,23H,4,6,8,10-13H2,1,3H3/t18-,19-,20+,21?,22?/m1/s1

14009-70-2SDS

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 13β-ethyl-3-methoxy-17α-ethynyl-gona-1,3,5(10)-trien-17β-ol

1.2 Other means of identification

Product number -
Other names 18-Methyl Mestranol

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:14009-70-2 SDS

14009-70-2Downstream Products

14009-70-2Relevant articles and documents

Preparation method of levonorgestrel pharmacopoeia impurity V

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Paragraph 0010; 0018; 0023-0030, (2020/12/31)

The invention belongs to the technical field of pharmacy, and particularly relates to a preparation method of a levonorgestrel pharmacopoeia impurity V. The preparation method comprises the steps of by taking a compound 1 as an initial raw material, carrying out aromatization reaction, methylation reaction and ethynylation reaction to prepare the levonorgestrel pharmacopoeia impurity V; the aromatization method comprises the steps of dissolving the compound 1 with an organic solvent, adding lithium bromide, controlling the temperature to be -5 to 5 DEG C, then adding copper bromide at the temperature, heating to room temperature, reacting and treating to obtain a compound 2. The product obtained by the method is high in purity and yield, avoids generation of impurities, and provides a qualified reference substance for quality control of levonorgestrel.

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