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Acetic acid 1-(cyclohexylidenemethyl)vinyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

49833-95-6

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49833-95-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 49833-95-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,9,8,3 and 3 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 49833-95:
(7*4)+(6*9)+(5*8)+(4*3)+(3*3)+(2*9)+(1*5)=166
166 % 10 = 6
So 49833-95-6 is a valid CAS Registry Number.

49833-95-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-cyclohexylideneprop-1-en-2-yl acetate

1.2 Other means of identification

Product number -
Other names 1-Propen-2-ol,3-cyclohexylidene-,acetate

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:49833-95-6 SDS

49833-95-6Downstream Products

49833-95-6Relevant academic research and scientific papers

Gold(I)-catalyzed isomerization of allenyl carbinol esters: An efficient access to functionalized 1,3-butadien-2-ol esters

Buzas, Andrea K.,Istrate, Florin M.,Gagosz, Fabien

, p. 985 - 988 (2007/10/03)

(Chemical Equation Presented) A study concerning the gold(I)-catalyzed rearrangement of diversely substituted allenyl carbinol esters into functionalized 1,3-butadien-2-ol esters is described. The mild conditions employed allow the efficient, rapid, and s

Palladium(II)-catalyzed SN2′ reactions of α-allenic acetates. Stereoconvergent synthesis of (Z,E)-2-bromo-1,3-dienes

Horvath, Attila,Baeckvall, Jan-E.

, p. 8120 - 8126 (2007/10/03)

The reaction of acetylated α-allenic alcohols with LiBr in the presence of 1.5 mol % of Pd(OAc)2 provides easy access to substituted (Z,E)-2-bromo-1,3-dienes in good yields with excellent diaste-reoselectivity. Both secondary and tertiary acetates as well as terminal and nonterminal allenes were studied to investigate the scope and the limitations of the reaction. A mechanism is proposed to clarify how a diastereomeric mixture of the starting compound is transformed into a single diastereomer of the product.

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