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90755-37-6

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90755-37-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90755-37-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,7,5 and 5 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 90755-37:
(7*9)+(6*0)+(5*7)+(4*5)+(3*5)+(2*3)+(1*7)=146
146 % 10 = 6
So 90755-37-6 is a valid CAS Registry Number.

90755-37-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name Furan, 2-(diethoxymethyl)tetrahydro-

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:90755-37-6 SDS

90755-37-6Downstream Products

90755-37-6Relevant articles and documents

Doping Pd/SiO2 with Na+: Changing the reductive etherification of CO to furan ring hydrogenation of furfural in ethanol

Long, Yinshuang,Wang, Yun,Wu, Haihong,Xue, Teng,Wu, Peng,Guan, Yejun

, p. 25345 - 25350 (2019/08/28)

The production of biofuels and chemicals by hydrogenation of furfural has attracted much attention recently. Herein the effect of Na+ doping on the catalytic performance of Pd/SiO2 in hydrogenation and reductive-etherification of furfural in ethanol was systematically studied. Two Pd/SiO2 catalysts with and without the modification by Na+ were prepared by impregnation and calcination. Their catalytic properties were compared for the hydrogenation of furfural and furfural diethyl acetal under mild conditions. The silanol groups on Pd/SiO2 catalysed the acetalization of furfural and alcohol and the resulted acetal underwent hydrogenolysis on Pd nanoparticles (NPs) with an average particle size of 8 nm, leading to a moderate yield (~58%) of furfuryl ethyl ether. Doping Na+ on Pd/SiO2 led to the diminishing of silanol groups as well as strong interaction between Na+ and Pd NPs. No acetalization occurred on Na+ modified Pd/SiO2 due to the exchange of H+ of Si-OH with Na+, thus the reductive etherification of CO group in furfural was completely inhibited. Meanwhile the hydrogenation of furan-ring over Na+ coordinated Pd NPs could proceed with very high selectivity (>90%) forming tetrahydrofurfural in high yield. Kinetics study on the hydrogenation of furfural diethyl acetal over Pd/SiO2 and Na+ doped Pd/SiO2 suggested that the Na+ greatly impeded the hydrogenolysis of C-O-C bond of acetal, while the hydrogenation of the furan ring took place selectively.

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