Cas 729592-63-6,(2R,3R,4R)-4-(tert-Butyl-dimethyl-silanyloxy)-2-methyl-6-phenylsulfanyl-tetrahydro-pyran-3-ol

729592-63-6

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Basic information

Product Name: (2R,3R,4R)-4-(tert-Butyl-dimethyl-silanyloxy)-2-methyl-6-phenylsulfanyl-tetrahydro-pyran-3-ol
Synonyms: (2R,3R,4R)-4-(tert-Butyl-dimethyl-silanyloxy)-2-methyl-6-phenylsulfanyl-tetrahydro-pyran-3-ol
CAS NO:729592-63-6
Molecular Formula:
Molecular Weight: 354.586
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: (2R,3R,4R)-4-(tert-Butyl-dimethyl-silanyloxy)-2-methyl-6-phenylsulfanyl-tetrahydro-pyran-3-ol(CAS DataBase Reference)
NIST Chemistry Reference: (2R,3R,4R)-4-(tert-Butyl-dimethyl-silanyloxy)-2-methyl-6-phenylsulfanyl-tetrahydro-pyran-3-ol(729592-63-6)
EPA Substance Registry System: (2R,3R,4R)-4-(tert-Butyl-dimethyl-silanyloxy)-2-methyl-6-phenylsulfanyl-tetrahydro-pyran-3-ol(729592-63-6)

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: 729592-63-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 729592-63-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,2,9,5,9 and 2 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 729592-63:
(8*7)+(7*2)+(6*9)+(5*5)+(4*9)+(3*2)+(2*6)+(1*3)=206
206 % 10 = 6
So 729592-63-6 is a valid CAS Registry Number.

729592-63-6Upstream product

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729592-63-6Relevant academic research and scientific papers

The significant effect of the carbohydrate structures on the DNA photocleavage of the quinoxaline-carbohydrate hybrids

Toshima, Kazunobu,Ozawa, Tomohiro,Kimura, Tomonori,Matsumura, Shuichi

, p. 2777 - 2779 (2004)

The novel DNA interactive quinoxaline-carbohydrate hybrids possessing disaccharides as the carbohydrate moieties were designed and synthesized, and their DNA photocleaving abilities were evaluated in order to examine the effect of the disaccharide structu

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