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126146-63-2

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126146-63-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 126146-63-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,1,4 and 6 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 126146-63:
(8*1)+(7*2)+(6*6)+(5*1)+(4*4)+(3*6)+(2*6)+(1*3)=112
112 % 10 = 2
So 126146-63-2 is a valid CAS Registry Number.

126146-63-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (9R,10S)-3-oxo-panaxydol

1.2 Other means of identification

Product number -
Other names 9,10-epoxy-1-heptadecene-4,6-diyn-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:126146-63-2 SDS

126146-63-2Downstream Products

126146-63-2Relevant articles and documents

Polyacetylene analogs, isolated from hairy roots of Panax ginseng, inhibit Acyl-CoA: Cholesterol acyltransferase

Kwon, Byoung-Mog,Ro, Sook-Hee,Kim, Mi-Kyung,Nam, Ji-Youn,Jung, Hyun-Ju,Lee, Ihn-Rhan,Kim, Young-Kook,Bok, Song-Hae

, p. 552 - 553 (1997)

In the course of our screening program for acylCoA:cholesterol acyltransferase (ACAT) inhibitors from Korean herbal medicines, ACAT inhibitors were isolated from the hairy roots of Panax ginseng (Araliaceae) and identified as panaxynol, panaxydol, panaxydiol, and panaxytriol. These active compounds inhibit rat liver ACAT with IC50 values of 94, 80, 45 and 79 μM, respectively.

Synthesis of panax acetylenes: Chiral syntheses of acetylpanaxydol, PQ-3 and panaxydiol

Satoh, Mitsuru,Watanabe, Mitsuo,Kawahata, Masatoshi,Mohri, Kunihiko,Yoshida, Yuki,Isobe, Kimiaki,Fujimoto, Yasuo

, p. 418 - 421 (2007/10/03)

Acetylpanaxydol (1-Ac), PQ-3 (2) and panaxydiol (3) and their optical isomers were synthesized from L-(+)-diethyl tartrate. The absolute configurations of 1-Ac, 2 and 3 were determined to be 1-Ac (3R,9R,10S), 2 (9R,10S) and 3 (3R,10S), respectively, by comparisons of their optical rotations and the NMR data of their MTPA esters with those of natural products.

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