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101765-35-9

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101765-35-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 101765-35-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,7,6 and 5 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 101765-35:
(8*1)+(7*0)+(6*1)+(5*7)+(4*6)+(3*5)+(2*3)+(1*5)=99
99 % 10 = 9
So 101765-35-9 is a valid CAS Registry Number.
InChI:InChI=1/C25H32O3/c1-22-6-3-14(26)11-19(22)24(9-10-24)13-16-17(22)4-7-23(2)21(16)15-12-18(15)25(23)8-5-20(27)28-25/h11,15-18,21H,3-10,12-13H2,1-2H3

101765-35-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 6,6-Emopc

1.2 Other means of identification

Product number -
Other names 6,6-Ethylene-15,16-methylene-3-oxo-17-pregn-4-ene-2,17-carbolactone

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:101765-35-9 SDS

101765-35-9Downstream Products

101765-35-9Relevant articles and documents

Aldosterone antagonists. 4. Synthesis and activities of steroidal 6,6-ethylene-15,16-methylene 17-spirolactones

Nickisch,Beier,Bittler,Elger,Laurent,Losert,Nishino,Schillinger,Wiechert

, p. 2464 - 2468 (1991)

Several steroidal 6,6-ethylene-15,16-methylene 17-spirolactones were synthesized to find new progestogens that exhibit both progestational and antimineralocorticoidal activities. The influence of substituents in the 10- and 13-position of the steroidal framework on both properties was investigated. It was found that only compound 12, carrying methyl groups at the 10- and 13-positions, possesses high progestational and antimineralocorticoidal activity.

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