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6265-26-5

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6265-26-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6265-26-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,6 and 5 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6265-26:
(6*6)+(5*2)+(4*6)+(3*5)+(2*2)+(1*6)=95
95 % 10 = 5
So 6265-26-5 is a valid CAS Registry Number.
InChI:InChI=1/C13H24O3/c14-11(5-7-12-3-1-9-15-12)6-8-13-4-2-10-16-13/h11-14H,1-10H2

6265-26-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,5-bis(oxolan-2-yl)pentan-3-ol

1.2 Other means of identification

Product number -
Other names 1,5-Bis(tetrahydro-2-furyl)-3-pentanol

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:6265-26-5 SDS

6265-26-5Downstream Products

6265-26-5Relevant articles and documents

Synthesis of Renewable Lubricant Alkanes from Biomass-Derived Platform Chemicals

Gu, Mengyuan,Xia, Qineng,Liu, Xiaohui,Guo, Yong,Wang, Yanqin

, p. 4102 - 4108 (2017/10/31)

The catalytic synthesis of liquid alkanes from renewable biomass has received tremendous attention in recent years. However, bio-based platform chemicals have not to date been exploited for the synthesis of highly branched lubricant alkanes, which are currently produced by hydrocracking and hydroisomerization of long-chain n-paraffins. A selective catalytic synthetic route has been developed for the production of highly branched C23 alkanes as lubricant base oil components from biomass-derived furfural and acetone through a sequential four-step process, including aldol condensation of furfural with acetone to produce a C13 double adduct, selective hydrogenation of the adduct to a C13 ketone, followed by a second condensation of the C13 ketone with furfural to generate a C23 aldol adduct, and finally hydrodeoxygenation to give highly branched C23 alkanes in 50.6 % overall yield from furfural. This work opens a general strategy for the synthesis of high-quality lubricant alkanes from renewable biomass.

INFLUENCE OF HYDROGEN PRESSURE ON THE RATE AND MECHANISM OF HYDROGENATION OF DIFURFURYLIDENEACETONE IN PRESENCE OF SKELETAL NICKEL-TITANIUM-ALUMINUM CATALYST

Mat'yakubov, R.,Abduganiev, E. G.,Kozhevnikov, V. S.

, p. 1976 - 1978 (2007/10/02)

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