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(20S)-Lupane-3β,29-diol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65556-58-3

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65556-58-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65556-58-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,5,5 and 6 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 65556-58:
(7*6)+(6*5)+(5*5)+(4*5)+(3*6)+(2*5)+(1*8)=153
153 % 10 = 3
So 65556-58-3 is a valid CAS Registry Number.

65556-58-3SDS

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 (20S)-lupane-3β,29-diol

1.2 Other means of identification

Product number -
Other names (1R,3aR,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-1-((S)-2-Hydroxy-1-methyl-ethyl)-3a,5a,5b,8,8,11a-hexamethyl-icosahydro-cyclopenta[a]chrysen-9-ol

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:65556-58-3 SDS

65556-58-3Downstream Products

65556-58-3Relevant academic research and scientific papers

New triterpene constituents, foliasalacins A1-A4, B1-B3, and C, from the leaves of Salacia chinensis

Yoshikawa, Masayuki,Zhang, Yi,Wang, Tao,Nakamura, Seikou,Matsuda, Hisashi

, p. 915 - 920 (2008)

Four dammarane-type, three lupane-type, and an oleanane-type triterpenes named foliasalacins A1 (1), A2 (2), A3 (3), A4 (4), B1 (5), B2 (6), B3 (7), and C (8) were isolated from

Lichens and Fungi. Part 17. The Synthesis and Absolute Configuration at C-20 of the (R)- and (S)-Epimers of Some 29-Substituted Lupane Derivatives and of some 30-Norlupan-20-ol Derivatives and the Crystal Structure of (20R)-3β-Acetoxylupan-29-ol.

Corbett, Edward R.,Cong, Aimy N. T.,Wilkins, Alistair L.,Thomson, Ralph, A.

, p. 2051 - 2056 (2007/10/02)

The absolute configurations at C-20 of the (R)- and (S)-aldehydes (10a), (10b), alcohols (11a), (11b), (13a), and (13b) and acids (12a), (12b), (14a), and (14b) derived from 3β-acetoxylup-20(29)-ene (8), via the epoxide (7), have been established by a combination of physical, spectral and X-ray crystallographic procedures, as have the configurations at C-20 of the (R)- and (S)-3β-acetoxy- and 3β-hydroxy-30-norlupan-20-ols (20a), (20b) and (21a), (21b).Anomalies in the literature are identified and rationalized.

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