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4709-59-5

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4709-59-5 Usage

Synthesis Reference(s)

Tetrahedron Letters, 25, p. 3247, 1984 DOI: 10.1016/S0040-4039(01)91022-6

Check Digit Verification of cas no

The CAS Registry Mumber 4709-59-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,0 and 9 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4709-59:
(6*4)+(5*7)+(4*0)+(3*9)+(2*5)+(1*9)=105
105 % 10 = 5
So 4709-59-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H16O2/c1-2-12-10(11)8-9-6-4-3-5-7-9/h6H,2-5,7-8H2,1H3

4709-59-5SDS

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 ethyl 2-(cyclohexen-1-yl)acetate

1.2 Other means of identification

Product number -
Other names ethyl cyclohexen-1-ylacetate

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:4709-59-5 SDS

4709-59-5Relevant articles and documents

Jorgenson,Patumtevapibal

, p. 489 (1970)

Synthesis of Fasicularin

Kaga, Atsushi,Tnay, Ya Lin,Chiba, Shunsuke

supporting information, p. 3506 - 3508 (2016/07/26)

The synthesis of a tricyclic marine alkaloid, fasicularin, was accomplished. Stereoselective synthesis of the aza-spirocyclic BC-ring precursor and ensuing construction of the A-ring with stereocontrolled installation of the C2 hexyl group feature prominently in the synthesis.

BF3-promoted synthesis of spiroindenyl heterocycles

Chang, Meng-Yang,Lin, Chung-Han,Chen, Yeh-Long,Hsu, Ru-Ting,Chang, Ching-Yao

scheme or table, p. 3154 - 3158 (2010/08/07)

An easy and straightforward synthesis of spiroindenyl heterocycles by the repeated treatment of boron trifluoride etherate (BF3-OEt2) is reported. The overall transformation from ketones 1 to spiro-fused indenes 3 proceeds via Wittig olefination, deconjugation, Grignard addition, and intramolecular electrophilic cyclization in moderate yields. It presents a novel rearrangement reaction catalyzed by boron trifluoride etherate and broadens the scope of application.

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