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Cyclohexanecarboxylic acid, 2-ethenyl-, trans- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 180908-13-8 Structure
  • Basic information

    1. Product Name: Cyclohexanecarboxylic acid, 2-ethenyl-, trans- (9CI)
    2. Synonyms: Cyclohexanecarboxylic acid, 2-ethenyl-, trans- (9CI)
    3. CAS NO:180908-13-8
    4. Molecular Formula: C9H14O2
    5. Molecular Weight: 154.20626
    6. EINECS: N/A
    7. Product Categories: CARBOXYLICACID
    8. Mol File: 180908-13-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Cyclohexanecarboxylic acid, 2-ethenyl-, trans- (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: Cyclohexanecarboxylic acid, 2-ethenyl-, trans- (9CI)(180908-13-8)
    11. EPA Substance Registry System: Cyclohexanecarboxylic acid, 2-ethenyl-, trans- (9CI)(180908-13-8)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 180908-13-8(Hazardous Substances Data)

180908-13-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 180908-13-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,0,9,0 and 8 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 180908-13:
(8*1)+(7*8)+(6*0)+(5*9)+(4*0)+(3*8)+(2*1)+(1*3)=138
138 % 10 = 8
So 180908-13-8 is a valid CAS Registry Number.

180908-13-8SDS

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 (1R,2S)-2-ethenylcyclohexane-1-carboxylic acid

1.2 Other means of identification

Product number -
Other names -

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:180908-13-8 SDS

180908-13-8Downstream Products

180908-13-8Relevant articles and documents

Preparation of cyclic imides from alkene-tethered amides: Application of homogeneous Cu(ii) catalytic systems

Chen, Suqing,Liu, Zhenghui,Mu, Tiancheng,Ou, Hualin,Tan, Xingxing,Wang, Peng,Yan, Zhenzhong,Yu, Dongkun,Zhao, Xinhui

, p. 7698 - 7707 (2020/03/13)

A Cu-based homogeneous catalytic system was proposed for the preparation of imides from alkene-tethered amides. Here, O2 acted as a terminal oxidant and a cheap and easily available oxygen source. The cleavage of CC bonds and the formation of C

A palladium-catalyzed aminoalkynylation strategy towards bicyclic heterocycles: Synthesis of (±)-trachelanthamidine

Nicolai, Stefano,Piemontesi, Cyril,Waser, Jerome

supporting information; experimental part, p. 4680 - 4683 (2011/06/23)

Sweet cyclizations: The synthesis of pyrrolizidines and indolizidines has been achieved. Olefins were subjected to an intramolecular palladium-catalyzed aminoalkynylation with the hypervalent iodine reagent TIPS-EBX. After removal of the protecting group, a two-step cyclization sequence and subsequent reduction led to the natural product (±)-trachelanthamidine (see scheme; TIPS-EBX=triisopropylsilyl ethynylbenziodoxolone).

Photoreactions of γ,δ-unsaturated chromium carbene complexes

Moser, William H.,Hegedus, Louis S.

, p. 7873 - 7880 (2007/10/03)

A number of functionalized γ,δ-unsaturated chromium carbene complexes were synthesized, and their photochemistry was studied. Photolysis of carbene complexes 5 and 17 induced intramolecular [2 + 2] cycloaddition to afford cyclobutanones 6 and 18, respectively. If the photoreactions were not run in thoroughly degassed solvents, small amounts of lactones 7 and 19 were obtained as well. Cyclobutanones 6 and 18 were stable once isolated, but underwent an acid-catalyzed Pinacol rearrangement/hydrolysis transformation in acidic solution to afford novel α-hydroxy-substituted bicyclo[3.1.0]hexanone compounds 20 and 21. Photolysis of cyclopropyl carbene complex 28 induced a vinylcyclopropyl rearrangement involving the photogenerated ketene moiety to provide α-alkoxy cyclopentenone 29.

CLAISEN-REARRANGEMENT-MEDIATED RING CONTRACTION OF MACROCYCLIC LACTONES A NEW APPROACH TO CARBOCYCLES AND HETEROCYCLES

Funk, Raymond L.,Abelman, Matthew, M.,Munger, John D.

, p. 2831 - 2846 (2007/10/02)

Macrocyclic ketene acetals 3 undergo Claisen rearrangements smoothly and constitute a viable and general approach to hetero- or carbocyclic ring systems 4.This novel ring contraction process is subject to high internal asymmetric induction (cf. lactones 7 -> carbocycles 8) as well as relative asymmetric induction in the rearrangements of ketene acetals derived from lactones 18, 23 and 27.Finally, N-benzoylmeroquinene methyl ester (37) was prepared to demonstrate the potential of this methodology in heterocycle synthesis.

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