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(E)-(1R,2R)-2-Benzyloxy-1-(R)-1,4-dioxa-spiro[4.5]dec-2-yl-5,5-dimethyl-hex-3-en-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

345892-01-5

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345892-01-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 345892-01-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,5,8,9 and 2 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 345892-01:
(8*3)+(7*4)+(6*5)+(5*8)+(4*9)+(3*2)+(2*0)+(1*1)=165
165 % 10 = 5
So 345892-01-5 is a valid CAS Registry Number.

345892-01-5SDS

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 (1R,2R,E)-2-(benzyloxy)-5,5-dimethyl-1-((R)-1,4-dioxaspiro[4.5]decan-2-yl)hex-3-en-1-ol

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:345892-01-5 SDS

345892-01-5Downstream Products

345892-01-5Relevant academic research and scientific papers

Reactivity of γ-benzyloxyallyltins with cyclohexylidene glyceraldehydes

Fliegel, Florian,Beaudet, Isabelle,Quintard, Jean-Paul

, p. 383 - 387 (2007/10/03)

Benzyloxyallyltributyltins were obtained in 50-80% yield by SN2′ reaction of alkyl-cyanocuprates with 3,3-dibenzyloxy-1-tributylstannylprop-1-ene in the presence of boron trifluoride. They reacted with cyclohexylidene glyceraldehyde in the presence of different Lewis acids and the obtained diastereomeric adducts were unambiguously identified after an ozonolysis/deprotection sequence by comparison with authentic aldopentoses. The mechanisms are briefly discussed as well as the relationship of the configuration of the reagents to the selectivity of the allylstannation reaction.

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