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FURFURAL-A-D1 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

42220-86-0

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42220-86-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 42220-86-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,2,2 and 0 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 42220-86:
(7*4)+(6*2)+(5*2)+(4*2)+(3*0)+(2*8)+(1*6)=80
80 % 10 = 0
So 42220-86-0 is a valid CAS Registry Number.

42220-86-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name FURFURAL-A-D1

1.2 Other means of identification

Product number -
Other names <12>Annulen

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:42220-86-0 SDS

42220-86-0Relevant academic research and scientific papers

Synthesis of furfural from xylose and xylan

Binder, Joseph B.,Blank, Jacqueline J.,Cefali, Anthony V.,Raines, Ronald T.

, p. 1268 - 1272 (2010)

Furans from pentoses: Pentose-derived furfural is a commodity chemical produced from lignocellulose. A new route to furfural from renewable carbohydrates uses chromium catalysts under mild conditions to avail a chemical mechanism distinct from the usual acid catalysis. Applicable to both xylose and xylan, this new method offers an advantageous route to biomass-derived chemicals.

A Practical Large Scale Chemical Synthesis of Chiral Glycines

Ramalingam, Kondareddiar,Nanjappan, Palaniappagownder,Kalvin, Douglas M.,Woodard, Ronald W.

, p. 5597 - 5604 (2007/10/02)

(R)- and (S)-2H>glycine of high chiral purity were synthesized in large quantities in ca.40percent overall yield from readily available starting materials via a totally chemical procedure.Reduction of either 2H>-furfural or 2H>-4-methoxybenzaldehyde with either (+) or (-)-B-isopinocampheyl-9-borabicyclononane gave chiral arylmethyl alcohols which were converted into their respective phthaloyl amino derivatives of the opposite configuration at the methylene carbon via the Mitsunobu reaction.The aromatic groups were oxidatively unmasked to give their corresponding glycine derivatives by either ozone or ruthenium tetraoxide oxidation.

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