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methyl (E)-non-6-enoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

40709-04-4

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40709-04-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 40709-04-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,7,0 and 9 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 40709-04:
(7*4)+(6*0)+(5*7)+(4*0)+(3*9)+(2*0)+(1*4)=94
94 % 10 = 4
So 40709-04-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H18O2/c1-3-4-5-6-7-8-9-10(11)12-2/h4-5H,3,6-9H2,1-2H3/b5-4+

40709-04-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl (E)-non-6-enoate

1.2 Other means of identification

Product number -
Other names EINECS 255-049-2

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:40709-04-4 SDS

40709-04-4Downstream Products

40709-04-4Relevant academic research and scientific papers

Stereoselective syntheses of Sex Pheromone of Mediterranean Fruitfly and Alarm Pheromone of Ants

Joshi, N. N.,Mamdapur, V. R.,Chadha, M. S.

, p. 577 - 579 (2007/10/02)

Facile synthetic routes to the sex pheromone components (Ia and Ib) of Mediterranean fruitfly, and te alarm pheromone (II) of ants in various species, are described.The key intermediates (1 and 2) for these syntheses, are derived from tetrahydrofurfuryl alcohol.Bromination of 1, and alkylation of dimethyl malonate with the resulting bromide (3), lead to Ia which on LAH reduction affords Ib.Whereas, oxidation of 2 followed by olefination with (i-propylidene)triphenylphosphorane, and subsequent deketalisation completes the synthesis of II.

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