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Factory Supply 3-isopropylidene-1-methylcyclohexene
Cas No: 17092-80-7
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Ality Chemical Corporation
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Cyclohexene,1-methyl-3-(1-methylethylidene)-
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Hangzhou J&H Chemical Co., Ltd.
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Cyclohexene,1-methyl-3-(1-methylethylidene)-
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yuyongmei
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17092-80-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17092-80-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,0,9 and 2 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 17092-80:
(7*1)+(6*7)+(5*0)+(4*9)+(3*2)+(2*8)+(1*0)=107
107 % 10 = 7
So 17092-80-7 is a valid CAS Registry Number.

InChI:InChI=1/C10H16/c1-8(2)10-6-4-5-9(3)7-10/h7H,4-6H2,1-3H3

17092-80-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name	1-methyl-3-propan-2-ylidenecyclohexene

1.2 Other means of identification

Product number	-
Other names	Sylveterpinolene

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:17092-80-7 SDS

17092-80-7Upstream product

17092-80-7Downstream Products

17092-80-7Relevant articles and documents

STABLE CARBOCATIONS FROM TERPENOIDS. IV. GENERATION OF STABLE IONS FROM SOME MONOTERPENES OF THE MENTAHNE AND CARANE SERIES

Popova, L. A.,Bardyshev, I. I.,Korchagina, D. V.,Dubovenko, Zh. V,Gatilov, Yu. V.,Barkhash, V. A.

, p. 709 - 720 (2007/10/02)

Stable carbocations were generated for the first time from momoterpenes of the menthane and carane-dipentene series, terpinolene, α and γ-terpinenes, isomeric p-menthenes, cis- and trans-caranes, and silvestrene.Their structures, reactions with nucleophiles, and certain rearrangements were studied.Differences were noted in the reactivity of the substrates in superacids and under conditions of acid catalysis

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CAS

17092-80-7