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36307-17-2

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36307-17-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36307-17-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,3,0 and 7 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 36307-17:
(7*3)+(6*6)+(5*3)+(4*0)+(3*7)+(2*1)+(1*7)=102
102 % 10 = 2
So 36307-17-2 is a valid CAS Registry Number.

36307-17-2SDS

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 dehydro-diconiferyl aldehyde

1.2 Other means of identification

Product number -
Other names Aldehyd des Dehydro-diconiferylalkohols

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:36307-17-2 SDS

36307-17-2Upstream product

36307-17-2Downstream Products

36307-17-2Relevant articles and documents

Selective oxidation of lignin model compounds

Gao, Ruili,Li, Yanding,Kim, Hoon,Mobley, Justin K.,Ralph, John

, p. , 2045 (2018)

Lignin, the planet’s most abundant renewable source of aromatic compounds, is difficult to degrade efficiently to well-defined aromatics. We developed a microwave-assisted catalytic Swern oxidation system using an easily prepared catalyst, MoO2Cl2(DMSO)2, and DMSO as the solvent and oxidant. It demonstrated high efficiency in transforming lignin model compounds containing the units and functional groups found in native lignins. The aromatic ring substituents strongly influenced the selectivity of β-ether phenolic dimer cleavage to generate sinapaldehyde and coniferaldehyde, monomers not usually produced by oxidative methods. Time-course studies on two key intermediates provided insight into the reaction pathway. Owing to the broad scope of this oxidation system and the insight gleaned with regard to its mechanism, this strategy could be adapted and applied in a general sense to the production of useful aromatic chemicals from phenolics and lignin.

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