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Pentane, 1,1,3,5,5-pentaethoxy-, also known as 1,1,3,5,5-pentaethoxypentane, is a chemical compound with the molecular formula C11H26O5. It is an ether derivative of pentane, where five ethoxy groups (C2H5O) are attached to the carbon atoms at positions 1, 1, 3, 5, and 5. Pentane, 1,1,3,5,5-pentaethoxy- is a colorless liquid with a low melting point and boiling point, and it is soluble in organic solvents. Due to its unique structure, it has potential applications in various chemical reactions and as a solvent in industrial processes. However, it is essential to handle Pentane, 1,1,3,5,5-pentaethoxy- with care, as it may have hazardous properties and require proper safety measures during storage and use.

5870-87-1

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5870-87-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5870-87-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,7 and 0 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5870-87:
(6*5)+(5*8)+(4*7)+(3*0)+(2*8)+(1*7)=121
121 % 10 = 1
So 5870-87-1 is a valid CAS Registry Number.

5870-87-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,3,5,5-pentaethoxy-pentane

1.2 Other means of identification

Product number -
Other names 3-ethoxy-glutaraldehyde bis-diethylacetal

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:5870-87-1 SDS

5870-87-1Relevant academic research and scientific papers

Enantioselective Saponification of Diacetates of 2-Nitro-1,3-propanediols by Pig-Liver Esterase and Preparation of Enantiomerically Pure Derivatives of 2-Nitro-allylic Alcohols (Chiral Multiple-Coupling Reagents)

Eberle, Martin,Egli, Martin,Seebach, Dieter

, p. 1 - 23 (2007/10/02)

The reproducible enantioselective saponification of open-chain and cyclic diacetates of meso-2-nitro-1,3-propanediols (see 4b-13b) with pig-liver esterase (PLE) gives monoacetates (see 4c-13c) of >95percent enantiomeric excess.The Re enantiotopic acetate group appears to be saponified preferentially, as proved by the X-ray crystal structure analysis of three camphanoates 4d, 6d, and 7d.Elimination of H2O or AcOH from the hydroxy acetates thus available gives derivatives of nitro-allylic alcohols (see 20-24, 27, and 29) which are subjected to diastereoselective Michael additions or SN2' substitutions.

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