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66348-47-8

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66348-47-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66348-47-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,3,4 and 8 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 66348-47:
(7*6)+(6*6)+(5*3)+(4*4)+(3*8)+(2*4)+(1*7)=148
148 % 10 = 8
So 66348-47-8 is a valid CAS Registry Number.

66348-47-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2(E)-Undecen-4-ol

1.2 Other means of identification

Product number -
Other names 2-undecen-4-ol

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:66348-47-8 SDS

66348-47-8Relevant articles and documents

Synthesis of allylic and homoallylic alcohols from unsaturated cyclic ethers using a mild and selective C-O reduction approach

MacK, Daniel J.,Guo, Boying,Njardarson, Jon T.

, p. 7844 - 7846 (2012/09/05)

Unsaturated cyclic ethers can be mildly and selectively reduced with catalytic amounts of B(C6F5)3 in the presence of an alkylsilane. The allylic position is preferentially reduced with minimal or no scrambling of olefin geometry. For electronically equivalent substrates, steric factors guide the reducing agent to the least substituted site.

ORGANOMANGANESE (II) REAGENTS XVIII: COPPER-CATALYZED 1,4-ADDITION OF ORGANOMANGANESE CHLORIDE COMPOUNDS TO CONJUGATED ETHYLENIC ALDEHYDES.

Cahiez, Gerard,Alami, Mouad

, p. 7365 - 7368 (2007/10/02)

Organomanganese chlorides react with β-mono or β,β-bisubstituted α,β-ethylenic aldehydes in the presence of a catalytic amount of copper chloride to give good yields of 1,4-addition products in THF at -30 deg C.

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