Cas 190258-23-2,1,3-Dioxolane-4,5-dimethanol, 2,2-dimethyl-, bis(4-methylbenzenesulfonate), (4R,5S)-rel-

190258-23-2

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Basic information

Product Name: 1,3-Dioxolane-4,5-dimethanol, 2,2-dimethyl-, bis(4-methylbenzenesulfonate), (4R,5S)-rel-
Synonyms:
CAS NO:190258-23-2
Molecular Formula: C21H26O8S2
Molecular Weight: 470.565
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: 1,3-Dioxolane-4,5-dimethanol, 2,2-dimethyl-, bis(4-methylbenzenesulfonate), (4R,5S)-rel-(CAS DataBase Reference)
NIST Chemistry Reference: 1,3-Dioxolane-4,5-dimethanol, 2,2-dimethyl-, bis(4-methylbenzenesulfonate), (4R,5S)-rel-(190258-23-2)
EPA Substance Registry System: 1,3-Dioxolane-4,5-dimethanol, 2,2-dimethyl-, bis(4-methylbenzenesulfonate), (4R,5S)-rel-(190258-23-2)

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: 190258-23-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 190258-23-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,0,2,5 and 8 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 190258-23:
(8*1)+(7*9)+(6*0)+(5*2)+(4*5)+(3*8)+(2*2)+(1*3)=132
132 % 10 = 2
So 190258-23-2 is a valid CAS Registry Number.

190258-23-2Upstream product

190258-23-2Downstream Products

176780-14-6 1,4-bis-O-tosyl-meso-erythritol

190258-23-2Relevant academic research and scientific papers

Stereodependent fusion and fission of vesicles: Calcium binding of synthetic gemini phospholipids containing two phosphate groups

Sommerdijk,Hoeks,Synak,Feiters,Nolte,Zwanenburg

, p. 4338 - 4344 (1997)

Three different stereoisomers of a phosphatidic acid analog bearing two phosphate groups have been synthesized from tartaric acid and erythritol. The obtained diastereomeric gemini surfactants differ in their aggregation behavior due to the different spat

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