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135710-38-2

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135710-38-2 Usage

General Description

Methyl 3,5-bis(allyloxy)benzenecarboxylate is a chemical compound with the molecular formula C15H16O4. It is a white solid with a molecular weight of 260.28 g/mol. This chemical is commonly used in the synthesis of various organic compounds and is often employed as a reagent in organic chemistry reactions. It is also used in the production of pharmaceuticals and is an important intermediate in the manufacturing of various other chemical products. Methyl 3,5-bis(allyloxy)benzenecarboxylate is considered to be a potentially hazardous material and should be handled and stored with care in accordance with safety guidelines and regulations.

Check Digit Verification of cas no

The CAS Registry Mumber 135710-38-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,7,1 and 0 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 135710-38:
(8*1)+(7*3)+(6*5)+(5*7)+(4*1)+(3*0)+(2*3)+(1*8)=112
112 % 10 = 2
So 135710-38-2 is a valid CAS Registry Number.
InChI:InChI=1/C14H16O4/c1-4-6-17-12-8-11(14(15)16-3)9-13(10-12)18-7-5-2/h4-5,8-10H,1-2,6-7H2,3H3

135710-38-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 3,5-bis(prop-2-enoxy)benzoate

1.2 Other means of identification

Product number -
Other names methylbisallyloxybenzenecarboxylate

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:135710-38-2 SDS

135710-38-2Relevant articles and documents

Green synthesis of (R)-terbutaline for recyclable catalytic asymmetric transfer hydrogenation in ionic liquids

Uchimoto, Hitomi,Ikeda, Miki,Tanida, Saori,Ohhashi, Kayo,Chihar, Yoshiko,Shigeta, Takashi,Arimitsu, Kenji,Yamashit, Masayuki,Nishide, Kiyoharu,Kawasaki, Ikuo

, p. 389 - 395 (2017/04/14)

We synthesize optically active (R)-terbutaline 2, which is an anti-asthmatic drug, through recyclable catalytic asymmetric transfer hydrogenation (RCATH). Various chloroketones 4 were prepared and RCATH was performed on them. The products exhibit moderate

Thermally activated, single component epoxy systems

Unruh, David A.,Pastine, Stefan J.,Moreton, Jessica C.,Frechet, Jean M. J.

experimental part, p. 6318 - 6325 (2012/06/18)

A single component epoxy system in which the resin and hardener components found in many two-component epoxies are combined onto the same molecule is described. The single molecule precursor to the epoxy resin contains both multiple epoxide moieties and a

Synthesis of supercritical carbon dioxide soluble perfluorinated dendrons for surface modification

Luscombe, Christine K.,Proemmel, Steffen,Huck, Wilhelm T. S.,Holmes, Andrew B.,Fukushima, Hitoshi

, p. 5505 - 5513 (2008/02/09)

(Chemical Equation Presented) The rational design, synthesis, and characterization of a series of novel perfluorinated dendrons 14a,b, 25a,b, 26a,b, and 18 are described. The dendrimers were designed to have a thiol at the focal point for attachment to a gold surface to enable the fabrication of self-assembled monolayers (SAMs). Perfluorinated tails were attached to the periphery to provide solubility in supercritical carbon dioxide, and to increase the hydrophobicity and the stability of self-assembled monolayers formed. Mitsunobu reactions were utilized to provide high-yielding steps allowing large-scale production of the novel dendrimers.

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