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35507-09-6

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35507-09-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 35507-09-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,5,0 and 7 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 35507-09:
(7*3)+(6*5)+(5*5)+(4*0)+(3*7)+(2*0)+(1*9)=106
106 % 10 = 6
So 35507-09-6 is a valid CAS Registry Number.

35507-09-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (7Z)-7-hexadecene

1.2 Other means of identification

Product number -
Other names (Z)-Hexadec-7-ene

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:35507-09-6 SDS

35507-09-6Downstream Products

35507-09-6Relevant articles and documents

Synthesis of an unnatural anacardic acid analogue

Green, Ivan R.,Tocoli, Felismino E.

, p. 947 - 957 (2007/10/03)

The unnatural E isomer of anacardic acid 7 has been synthesized employing the following key steps: Swern oxidation of a diastereoisomeric mixture of β-hydroxyphosphine oxides 13a/b to the corresponding ketone 14 followed by stereo-specific reduction to th

Cross-Coupling Reaction of Alkyl- or Arylboronic Acid Esters with Organic Halides Induced by Thallium(I) Salts and Palladium-Catalyst

Sato, Makoto,Miyaura, Norio,Suzuki, Akira

, p. 1405 - 1408 (2007/10/02)

The cross-coupling reaction of alkylboronic acid esters with 1-alkenyl- or aryl halides is succesfully catalyzed by PdCl2 (dppf) or Pd(PPh3)4 in the presence of thallium(I) hydroxide or carbonate to give the corresponding alkenes or arenes in good yields.The coupling reaction of arylboronic acid esters with aryl halides under similar conditions to provide biaryls is also described.

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