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18736-82-8

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18736-82-8 Usage

General Description

1-Cyclohexyl-2-buten-1-ol is a chemical compound with the molecular formula C10H18O. It is a colorless liquid with a sweet floral odor, commonly used as a fragrance and flavoring agent. It is also known for its potential applications in the pharmaceutical and organic synthesis industries. The compound is composed of a cyclohexyl group and a butenol group, which gives it unique chemical properties and reactivity. 1-Cyclohexyl-2-buten-1-ol has been studied for its biological activities and potential use as an antiviral and antibacterial agent. Due to its versatile nature and desirable properties, this compound is a valuable addition to the arsenal of chemicals used in various industrial and scientific applications.

Check Digit Verification of cas no

The CAS Registry Mumber 18736-82-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,7,3 and 6 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 18736-82:
(7*1)+(6*8)+(5*7)+(4*3)+(3*6)+(2*8)+(1*2)=138
138 % 10 = 8
So 18736-82-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H18O/c1-2-6-10(11)9-7-4-3-5-8-9/h2,6,9-11H,3-5,7-8H2,1H3/b6-2-/t10-/m0/s1

18736-82-8 Well-known Company Product Price

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  • Alfa Aesar

  • (B20501)  1-Cyclohexyl-2-buten-1-ol, tech. 90%   

  • 18736-82-8

  • 5g

  • 570.0CNY

  • Detail
  • Alfa Aesar

  • (B20501)  1-Cyclohexyl-2-buten-1-ol, tech. 90%   

  • 18736-82-8

  • 25g

  • 1370.0CNY

  • Detail

18736-82-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-cyclohexylbut-2-en-1-ol

1.2 Other means of identification

Product number -
Other names 1-Cyclohexyl-2-buten-1-ol

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:18736-82-8 SDS

18736-82-8Relevant articles and documents

Tuning of α-Silyl Carbocation Reactivity into Enone Transposition: Application to the Synthesis of Peribysin D, E-Volkendousin, and E-Guggulsterone

Athawale, Paresh R.,Zade, Vishal M.,Rama Krishna, Gamidi,Reddy, D. Srinivasa

, p. 6642 - 6647 (2021/09/02)

A reliable method for enone transposition has been developed with the help of silyl group masking. Enantio-switching, substituent shuffling, and Z-selectivity are the highlights of the method. The developed method was applied for the first total synthesis of peribysin D along with its structural revision. Formal synthesis of E-guggulsterone and E-volkendousin was also claimed using a short sequence.

Copper-Catalyzed Enantioselective Conjugate Addition to α,β-Unsaturated Aldehydes with Various Organometallic Reagents

Goncalves-Contal, Sylvie,Gremaud, Ludovic,Palais, La?titia,Babel, Lucille,Alexakis, Alexandre

, p. 3301 - 3308 (2016/09/12)

β-Substituted aldehydes constitute a very important class of compounds found in nature. Synthesis of this motif can be envisioned by C-C bond formation on enals. For this purpose, we report herein the development of enantioselective copper-catalyzed conjugate addition of various organometallic reagents to α,β-unsaturated aldehydes with (R)-H8BINAP, (R)-TolBINAP, and (R)-SEGPHOS as chiral ligands. Three sets of conditions were successfully developed and several enals were used. Reactivity and regio- and enantioselectivities were strongly dependent on reaction conditions and substrates. Good to excellent regio- and enantioselectivities were obtained with zinc reagents R2Zn and aluminum reagents R3Al. However, the asymmetric conjugate addition of Grignard reagents afforded only moderate to good regio- and enantioselectivities.

Dihydrothiophenes containing quaternary stereogenic centres by sequential stereospecific rearrangements and ring-closing metathesis

Mingat, Ga?lle,McDouall, Joseph J. W.,Clayden, Jonathan

, p. 6754 - 6757 (2014/06/23)

Stereospecific [3,3]-sigmatropic rearrangement of O-substituted thiocarbamate derivatives of enantiopure allylic alcohols provides allylic thiocarbamates as single enantiomers. Intramolecular arylation by rearrangement of their allyllithium derivatives provides allylic tertiary thiols. Allylation and ring-closing metathesis gives 2,5-dihydrothiophenes containing sulfur-bearing quaternary centres. This journal is the Partner Organisations 2014.

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