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4-Heptanone, 3-(diphenylphosphinyl)-1-(2-methyl-1,3-dioxolan-2-yl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

104745-16-6

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104745-16-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 104745-16-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,7,4 and 5 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 104745-16:
(8*1)+(7*0)+(6*4)+(5*7)+(4*4)+(3*5)+(2*1)+(1*6)=106
106 % 10 = 6
So 104745-16-6 is a valid CAS Registry Number.

104745-16-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-diphenylphosphinoylnonane-2,6-dione ethylene acetal

1.2 Other means of identification

Product number -
Other names 3-(Diphenyl-phosphinoyl)-1-(2-methyl-[1,3]dioxolan-2-yl)-heptan-4-one

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:104745-16-6 SDS

104745-16-6Downstream Products

104745-16-6Relevant articles and documents

SYNTHESIS OF SINGLE ISOMERS (E OR Z) OF PROTECTED γ,δ-UNSATURATED KETONES BY THE HORNER-WITTIG REACTION

Cornish Christopher A.,Warren, Stuart

, p. 2585 - 2598 (2007/10/02)

The lithium derivative of the γ-diphenylphosphinoyl ketal (10a) added to aldehydes and ketones to give stable Horner-Wittig intermediates (11) which were separated and converted into single isomers (E or Z) or γ,δ-unsaturated ketals (12). erythro-Adducts (11) and hence Z-(12), were selectively formed by addition of aldehydes and threo adducts (11), and hence E-(12), by reduction of the corresponding α-diphenylphosphinoyl ketones (13), prepared by acylation of the same γ-diphenylphosphinoyl ketal (10a).

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