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57706-68-0

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  • methyl (4R)-4-[(3S,5S,8R,9S,10S,13R,14S,17R)-3-acetyloxy-4,4,10,13,14-pentamethyl-7,11-dioxo-2,3,5,6,8,9,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]pentanoate

    Cas No: 57706-68-0

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  • methyl (4R)-4-[(3S,5S,8R,9S,10S,13R,14S,17R)-3-acetyloxy-4,4,10,13,14-pentamethyl-7,11-dioxo-2,3,5,6,8,9,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]pentanoate cas 57706-68-0

    Cas No: 57706-68-0

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57706-68-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57706-68-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,7,0 and 6 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 57706-68:
(7*5)+(6*7)+(5*7)+(4*0)+(3*6)+(2*6)+(1*8)=150
150 % 10 = 0
So 57706-68-0 is a valid CAS Registry Number.

57706-68-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3β-Acetoxy-7,11-dioxo-4,4,14α-trimethyl-5α-cholan-24-oic acid methyl ester

1.2 Other means of identification

Product number -
Other names 3??-acetoxy-7,11-dioxo-25,26,27-trinor-lanostan-24-oic acid methyl ester

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

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Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:57706-68-0 SDS

57706-68-0Relevant articles and documents

SYNTHESIS OF KETO DERIVATIVES OF LANOSTANE-24-CARBOXYLIC ACID

Reshetova, I. G.,Tkhaper, R. K.,Kamernitskii, A. V.,Bogdanov, V. S.

, p. 607 - 609 (2007/10/02)

The oxidation of lanosterol by potassium permanganate and sodium periodate is a complex reaction with involvement of both the 24(25)-double bond and allylic positions (C7 and C11), leading to the formation of the corresponding ketoacids.

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