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2115-48-2

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  • [4,4,10,13,14-pentamethyl-17-(6-methylheptan-2-yl)-7-oxo-1,2,3,5,6,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-yl] acetate

    Cas No: 2115-48-2

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  • [4,4,10,13,14-pentamethyl-17-(6-methylheptan-2-yl)-7-oxo-1,2,3,5,6,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-yl] acetate cas 2115-48-2

    Cas No: 2115-48-2

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2115-48-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2115-48-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,1 and 5 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2115-48:
(6*2)+(5*1)+(4*1)+(3*5)+(2*4)+(1*8)=52
52 % 10 = 2
So 2115-48-2 is a valid CAS Registry Number.

2115-48-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name [4,4,10,13,14-pentamethyl-17-(6-methylheptan-2-yl)-7-oxo-1,2,3,5,6,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-yl] acetate

1.2 Other means of identification

Product number -
Other names -

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:2115-48-2 SDS

2115-48-2Relevant articles and documents

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Cavalla,McGhie

, p. 744,746 (1951)

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1H and 13C NMR Assignments for Lanostan-3β-ol Derivatives: Revised Assignments for Lanosterol

Emmons, Gary T.,Wilson, William K.,Schroepfer, George J. Jr

, p. 1012 - 1024 (2007/10/02)

1H and 13C NMR assignments are presented for 30 oxygenated lanostane derivatives, including lanosterol, dihydrolanosterol, 7-ketolanosterol, agnosterol, 24,25-epoxylanosterol, 8α,9α-epoxylanostan-3β-ol, three 15-oxygenated derivatives of lanost-7-en-3β-ol, lanostane-3β,7α-diol, lanostane-3B,9α-diol and their acetates.These assignments, which were largely determined by a combination of DEPT, one-bond and long-range 13C-1H chemical shift correlation and lanthanide-induced shift experiments, are not dependent on previously reported assignments, several of which were found to be incorrect. 1H and 13C acetylation shifts for lanostan-3β-ols were sufficiently invariant among the sterols studied that they were useful for assigning carbons in rings A and B.The acetylation shifts reported for lanostan-3β-ols were extended and partially revised.-- Key Words 1H and 13C NMR Oxygenated lanostane derivatives Spectral assignment Lanthanide-induced shifts Long-range HECTOR Acetylation shifts

Oxygen containing lanostan derivatives from wool wax

Brieskorn,Dertinger

, p. 960 - 967 (2007/10/05)

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