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117591-80-7

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117591-80-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 117591-80-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,5,9 and 1 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 117591-80:
(8*1)+(7*1)+(6*7)+(5*5)+(4*9)+(3*1)+(2*8)+(1*0)=137
137 % 10 = 7
So 117591-80-7 is a valid CAS Registry Number.
InChI:InChI=1/C15H26O/c1-12(2)10-15(16)13(3)7-5-8-14(15,4)11(12)6-9-13/h11,16H,5-10H2,1-4H3/t11-,13+,14-,15+/m0/s1

117591-80-7SDS

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 Ginsenol

1.2 Other means of identification

Product number -
Other names acetylginsenol

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:117591-80-7 SDS

117591-80-7Downstream Products

117591-80-7Relevant academic research and scientific papers

Reactions of caryophyllene, isocaryophyllene, and their epoxy derivatives with acetonitrile under ritter reaction conditions

Yarovaya,Korchagina,Rybalova,Gatilov,Polovinka,Barkhash

, p. 1593 - 1598 (2004)

Acid-catalyzed reactions between acetonitrile and caryophyllene, isocaryophyllene, caryophyllene 4β,5α-epoxide, and isocaryophyllene 4β,5β-epoxide affording optically active amides with a tricyclic skeleton were investigated. 2004 MAIK "Nauka/Interperiodica".

MOLECULAR REARRANGEMENTS OF NEOCLOVENE IN ACIDIC MEDIA. THE EFFECT OF THE NATURE OF THE MEDIUM ON THE PREFERRED DIRECTION IN MULTISTAGE CARBOCATIONIC REARRANGEMENTS

Khomenko, T. M.,Korchagina, D. V.,Gatilov, Yu. V.,Bagrayanskaya, I. Yu.,Rybalova, T. V.,et al.

, p. 493 - 516 (2007/10/02)

In the case of the transformations of neoclovene in media with various acidities it was discovered experimentally and confirmed by molecular-mechanical calculations, that the relative stability of the carbocations and the corresponding olefins varies in t

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