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67983-55-5

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67983-55-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67983-55-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,9,8 and 3 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 67983-55:
(7*6)+(6*7)+(5*9)+(4*8)+(3*3)+(2*5)+(1*5)=185
185 % 10 = 5
So 67983-55-5 is a valid CAS Registry Number.

67983-55-5SDS

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 11β-(p-methoxyphenyl)-17β-hydroxy-17α-ethynyl-4,9(10)-estradien-3-one

1.2 Other means of identification

Product number -
Other names 11β-p-methoxyphenyl-17β-hydroxy-17α-ethinyl-4,9-(10)-estradien-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:67983-55-5 SDS

67983-55-5Relevant articles and documents

Progesterone antagonists for the production of pharmaceutical agents for the treatment of dysfunctional uterine bleeding

-

, (2008/06/13)

Competitive progesterone antagonists (antigestagens) are suitable for the production of pharmaceutical agents for the treatment of forms of dysfunctional uterine bleeding (metrorrhagias, menorrhagias, hypermenorrhea).

REGIO AND STEREOSPECIFIC SYNTHESIS OF 11β-SUBSTITUTED 19-NORSTEROIDS. Influence of 11β-substitution on progesterone receptor affinity.

Belanger, A.,Philibert, D.,Teutsch, G.

, p. 361 - 382 (2007/10/02)

The convenient synthesis of a series of 11β-substituted 17-ethynyl-17β-hydroxy-4,9-estradien-3-ones and their corresponding estradiols is reported.Relative affinities for the progestin and estrogen receptors showed very specific interactions between the p

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