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344359-68-8

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344359-68-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 344359-68-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,4,3,5 and 9 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 344359-68:
(8*3)+(7*4)+(6*4)+(5*3)+(4*5)+(3*9)+(2*6)+(1*8)=158
158 % 10 = 8
So 344359-68-8 is a valid CAS Registry Number.

344359-68-8SDS

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 E-7-phenylhept-4-enoic acid

1.2 Other means of identification

Product number -
Other names -

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:344359-68-8 SDS

344359-68-8Downstream Products

344359-68-8Relevant articles and documents

Formation of COOH-Ylides, and Their Reactivities and Selectivities in Wittig Reactions

Suganuma, Yuta,Kobayashi, Yuichi

, p. 333 - 337 (2019/02/12)

Whereas two equivalents of base are typically required to prepare carboxylate (CO 2-) ylides [Ph 3 P + C - (H)-alk-CO 2- ] (alk = alkanediyl) from carboxy (CO 2 H) pho

Organoselenium-catalyzed synthesis of oxygen- and nitrogen-containing heterocycles

Guo, Ruizhi,Huang, Jiachen,Huang, Haiyan,Zhao, Xiaodan

supporting information, p. 504 - 507 (2016/02/18)

A new and efficient approach for the synthesis of oxygen and nitrogen heterocycles by organoselenium catalysis has been developed. The exo-cyclization proceeded smoothly under mild conditions with good functional group tolerance and excellent regioselectivity. Mechanistic studies revealed that 1-fluoropyridinium triflate is key for oxidative cyclization.

Pesticidal activity of functionalized alkenes

-

Page column 13-14, (2008/06/13)

The present invention provides non-peptide organic compounds that have a structure analogous to or reminiscent of the TMOF structure and have pesticidal activity. Thus the present invention concerns pesticidal compounds that inhibit digestion in pests by terminating or otherwise blocking synthesis of digestive enzymes by activating a TMOF receptor (collectively referred to herein as “pesticidal compounds”). The pesticidal compounds and other compounds of the present invention are usefully employed in the control of pests, particularly insect pests such as mosquitoes, which ingest blood.

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