Cas 110808-34-9,Toluene-4-sulfonic acid (3aR,5R,6R,6aR)-6-hydroxy-2,2,6-trimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-ylmethyl ester

110808-34-9

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Basic information

Product Name: Toluene-4-sulfonic acid (3aR,5R,6R,6aR)-6-hydroxy-2,2,6-trimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-ylmethyl ester
Synonyms: Toluene-4-sulfonic acid (3aR,5R,6R,6aR)-6-hydroxy-2,2,6-trimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-ylmethyl ester
CAS NO:110808-34-9
Molecular Formula:
Molecular Weight: 358.412
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 (3aR,5R,6R,6aR)-6-hydroxy-2,2,6-trimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-ylmethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Toluene-4-sulfonic acid (3aR,5R,6R,6aR)-6-hydroxy-2,2,6-trimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-ylmethyl ester(110808-34-9)
EPA Substance Registry System: Toluene-4-sulfonic acid (3aR,5R,6R,6aR)-6-hydroxy-2,2,6-trimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-ylmethyl ester(110808-34-9)

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: 110808-34-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 110808-34-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,8,0 and 8 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 110808-34:
(8*1)+(7*1)+(6*0)+(5*8)+(4*0)+(3*8)+(2*3)+(1*4)=89
89 % 10 = 9
So 110808-34-9 is a valid CAS Registry Number.

110808-34-9Upstream product

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110808-34-9Relevant academic research and scientific papers

Study on the diastereoselective synthesis of dithymidine phosphorothioates through a D-xylose derived chiral auxiliary and development of a novel catalyst

Lu,Just

, p. 9223 - 9227 (2007/10/03)

1,2-Di-O-isopropylidene-3-C-cyanoethyl-5-deoxy-5-isopropylamino-D-xylofuranos e 16a was synthesized. The use of 16a as a chiral auxiliary led to the diastereoselective formation of dithymidine phosphorothioate. The chiral auxiliary was easily removed by treatment with concentrated ammonia. 2-Mesityl-4,5-dicyanoimidazole displays higher diastereoselectivity than the 2-bromo-4,5-dicyanoimidazole in the coupling reaction. (C) 2000 Elsevier Science Ltd.

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