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106673-42-1

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106673-42-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 106673-42-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,6,7 and 3 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 106673-42:
(8*1)+(7*0)+(6*6)+(5*6)+(4*7)+(3*3)+(2*4)+(1*2)=121
121 % 10 = 1
So 106673-42-1 is a valid CAS Registry Number.

106673-42-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-1-benzyloxydec-2-ene

1.2 Other means of identification

Product number -
Other names [((E)-Dec-2-enyl)oxymethyl]-benzene

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:106673-42-1 SDS

106673-42-1Downstream Products

106673-42-1Relevant articles and documents

The Synthesis and Ring Opening Reactions of 1,10-Disubstituted-2,3 (R,R + S,S) Epoxy Decanes - A Route to Heterocyclic Prostaglandin Analogues.

Grayshan, Roger,Keal, Colin A.,Sackville, Michael A.

, p. 2501 - 2542 (2007/10/02)

Synthetic routes leading to (E)-1,10-di-derivatised dec-2-enes are outlined; in particular the syntheses of (E)-1-benzyloxy-10-methoxyethoxymethoxydec-2-ene and (E)-10-benzyloxy-1-methoxyethoxymethoxydec-2-ene are described.Ring opening reactions between 2-lithio-1,3-dithiane and the oxiranes derived from the above two decenes were studied and the ratio of isomeric dithianyl alcohols produced was shown to be influenced by the nature of the C-1 hydroxyl protecting group.These results are discussed in terms of co-ordinative interactions between the lithiodithiane reagent and the complementary oxygens of the substituted oxiranes.

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