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55255-64-6

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55255-64-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55255-64-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,2,5 and 5 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 55255-64:
(7*5)+(6*5)+(5*2)+(4*5)+(3*5)+(2*6)+(1*4)=126
126 % 10 = 6
So 55255-64-6 is a valid CAS Registry Number.

55255-64-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,4'-(2-oxa-propanediyl)-di-benzoic acid

1.2 Other means of identification

Product number -
Other names Dibenzylaether-dicarbonsaeure-(4.4')

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:55255-64-6 SDS

55255-64-6Relevant articles and documents

Reduction of carbonyl compounds promoted by silicon hydrides under the influence of trimethylsilyl-based reagents

Aizpurua, Jesus M.,Lecea, Begona,Palomo, Claudio

, p. 2342 - 2347 (2007/10/02)

The synthetic utility of hydrosilanes under the influence of trimethylsilyl-based reagents as new reducing systems is described. 1,1,3,3-Tetramethyldisiloxane (TMDS) reagent in combination with iodotrimethylsilane or bromotrimethylsilane produces alkyl halides from aldehydes in good to excellent yields.Polymethylhydrosiloxane (PMS) in the presence of iodotrimethylsilane also produces benzyl iodides in excellent yields.On the contrary, PMS reagent was found unsuitable for the synthesis of benzyl bromides.Similary, TMDS reagent in combination with trimethylsilyl triflate produces symmetrical ethers from aldehydes without concomitant formation of competitive products.Under similar conditions, PMS reagent failed to provide the expected symmetrical ethers and Friedel-Crafts products were formed.Reduction of quinones to hydroquinones is also described.

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