Cas 3515-98-8,2-(10-methoxycarbonyldecyl)-1,3-dioxolane

3515-98-8

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Basic information

Product Name: 2-(10-methoxycarbonyldecyl)-1,3-dioxolane
Synonyms: 2-(10-methoxycarbonyldecyl)-1,3-dioxolane
CAS NO:3515-98-8
Molecular Formula:
Molecular Weight: 272.385
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 2-(10-methoxycarbonyldecyl)-1,3-dioxolane(CAS DataBase Reference)
NIST Chemistry Reference: 2-(10-methoxycarbonyldecyl)-1,3-dioxolane(3515-98-8)
EPA Substance Registry System: 2-(10-methoxycarbonyldecyl)-1,3-dioxolane(3515-98-8)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 3515-98-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 3515-98-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,1 and 5 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3515-98:
(6*3)+(5*5)+(4*1)+(3*5)+(2*9)+(1*8)=88
88 % 10 = 8
So 3515-98-8 is a valid CAS Registry Number.

3515-98-8Upstream product

3515-98-8Downstream Products

3602-59-3 12-(2,4-dinitro-phenylhydrazono)-dodecanoic acid methyl ester

3515-98-8Relevant academic research and scientific papers

METHOD FOR PRODUCING ALDEHYDE FUNCTIONAL COMPOUNDS

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Page/Page column 6-7, (2012/02/03)

The invention relates to a method for producing aldehyde functional compounds by a cross-metathesis reaction of an olefinic compound having at least one hydroxy group and at least one C—C double bond with at least one at least monounsaturated fatty acid or at least one at least monounsaturated fatty acid derivative, in the presence of a metathesis catalyst at a maximum temperature of 180° C. and in the presence of at least one reagent that acts as a protective group-forming compound in relation to the aldehyde group of the aldehyde functional compounds.

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