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18088-97-6

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18088-97-6 Usage

Uses

β-Cyclolavandulic Acid is a proposed intermediate in the synthesis of 1,1,5,5-Tetramethyl-2-(1-methylethenyl)cyclohexane (T305630), which is analyzed in synthetic elastomers and natural rubber studies of cyclic oligomer formation in the copolymerization of isoprene with isobutylene.

Check Digit Verification of cas no

The CAS Registry Mumber 18088-97-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,0,8 and 8 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 18088-97:
(7*1)+(6*8)+(5*0)+(4*8)+(3*8)+(2*9)+(1*7)=136
136 % 10 = 6
So 18088-97-6 is a valid CAS Registry Number.

18088-97-6SDS

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 2,4,4-trimethylcyclohexene-1-carboxylic acid

1.2 Other means of identification

Product number -
Other names 2,4,4-Trimethyl-cyclohex-1-encarbonsaeure

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:18088-97-6 SDS

18088-97-6Relevant articles and documents

Transition metals in organic synthesis, Part 98.1 Transition metal mediated total synthesis of the potent neuronal cell protecting alkaloid (±)-lavanduquinocin

Froehner, Wolfgang,Reddy, Kethiri R.,Knoelker, Hans-Joachim

, p. 330 - 342 (2013/09/24)

An efficient total synthesis of (±)-lavanduquinocin, a potent neuronal cell protecting alkaloid from Streptomyces viridochromogenes, is reported. Key-steps are an iron-mediated one-pot construction of the carbazole framework and a nickel-mediated coupling reaction. ARKAT-USA, Inc.

An efficient synthetic method for β-cyclolavandulal and its corresponding alcohol

Oda, Mitsunori,Isobe, Atsushi,Hayashi, Masashi,Miyatake, Ryuta,Shimao, Ichiro,Kuroda, Shigeyasu

, p. 438 - 440 (2007/10/03)

3,3-Dimethylcyclohexanone (5) was efficiently converted to methyl β-cyclolavandulate (6) in 74% yield in three steps, one of which included the preparation of β-methyl α,β-unsaturated esters by coupling lithium dimethylcuprate with enol phosphates of β-ox

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