Cas 258336-12-8,Toluene-4-sulfonic acid (2S,4R,5R)-5-[1,3]dioxolan-2-yl-4-hydroxy-tetrahydro-furan-2-ylmethyl ester

258336-12-8

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Basic information

Product Name: Toluene-4-sulfonic acid (2S,4R,5R)-5-[1,3]dioxolan-2-yl-4-hydroxy-tetrahydro-furan-2-ylmethyl ester
Synonyms: Toluene-4-sulfonic acid (2S,4R,5R)-5-[1,3]dioxolan-2-yl-4-hydroxy-tetrahydro-furan-2-ylmethyl ester
CAS NO:258336-12-8
Molecular Formula:
Molecular Weight: 344.386
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: Toluene-4-sulfonic acid (2S,4R,5R)-5-[1,3]dioxolan-2-yl-4-hydroxy-tetrahydro-furan-2-ylmethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Toluene-4-sulfonic acid (2S,4R,5R)-5-[1,3]dioxolan-2-yl-4-hydroxy-tetrahydro-furan-2-ylmethyl ester(258336-12-8)
EPA Substance Registry System: Toluene-4-sulfonic acid (2S,4R,5R)-5-[1,3]dioxolan-2-yl-4-hydroxy-tetrahydro-furan-2-ylmethyl ester(258336-12-8)

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: 258336-12-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 258336-12-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,8,3,3 and 6 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 258336-12:
(8*2)+(7*5)+(6*8)+(5*3)+(4*3)+(3*6)+(2*1)+(1*2)=148
148 % 10 = 8
So 258336-12-8 is a valid CAS Registry Number.

258336-12-8Upstream product

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258336-12-8Relevant academic research and scientific papers

Divergent synthesis of two novel muscarine analogues from D-glucose

Popsavin, Velimir,Popsavin, Mirjana,Radi?, Ljubica,Beri?, Ostoja,?irin-Novta, Vera

, p. 9305 - 9308 (2007/10/03)

A divergent synthesis of two new muscarine analogues bearing the (5S)-dioxolanyl isosteric group was achieved starting from D-glucose, enabling access to libraries of potential muscarinic agonists or antagonists. The key step of the synthesis involved a r

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