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33741-15-0

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33741-15-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 33741-15-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,7,4 and 1 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 33741-15:
(7*3)+(6*3)+(5*7)+(4*4)+(3*1)+(2*1)+(1*5)=100
100 % 10 = 0
So 33741-15-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H12O2/c1-3-4-5-6-7-8(9)10-2/h3-5H,1,6-7H2,2H3/b5-4+

33741-15-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name METHYL HEPTA-4,6-DIENOATE

1.2 Other means of identification

Product number -
Other names Methyltrans-4,6-heptadienoate

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:33741-15-0 SDS

33741-15-0Relevant articles and documents

Synthesis of the A/E/F sections of conaconitine, napelline and related diterpenoid alkaloids of the aconitine group

Baillie, Lynn C.,Batsanov, Andrei,Bearder, John R.,Whiting, Donald A.

, p. 3471 - 3478 (1998)

The tricyclic amines (±)-2; R = H and R = Me with five stereogenic centres, representing the A/E/F ring system of the title alkaloids, have been synthesised from penta-1,4-dien-3-ol in eight (overall yield 20%) and nine steps (overall yield 16%) respectively.

Efficient syntheses of the polyene fragments present in amphidinols

Cossy, Janine,Tsuchiya, Tomoki,Ferrié, Laurent,Reymond, Sébastien,Kreuzer, Thomas,Colobert, Fran?oise,Jourdain, Pierre,Markó, István E.

, p. 2286 - 2288 (2008/02/09)

The C53-C67 and C53-C65 polyene fragments of amphidinols have been synthesized in an efficient and convergent fashion from sorbic acid in good overall yields (30-31%) by employing a chemoselective cross-metathesis of a Weinreb amide and a Julia-Kocienski

Photochemistry of 2-Fluoro-2-alkylcyclohexanones. Drastic Effect of Fluorine Substitution

Reinholdt, Karin,Margaretha, Paul

, p. 119 - 122 (2007/10/02)

In the photreactions of 3-(2-oxocyclohexyl)-propionic acid derivatives 1 a pronounced effect of fluorine substitution is found on the ratio of a) Norrish II vs.Norrish I products; b) cyclization vs. cleavage of the Norrish II biradical; c) ketene vs. unsaturated aldehyde formation from the Norrish I biradical.

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