Cas 615250-74-3,2,2-Dimethyl-propionic acid (R)-3-((2R,4R,5S,6R)-5-acetoxy-4-dimethylamino-6-methyl-tetrahydro-pyran-2-yloxy)-2-(toluene-4-sulfonyloxy)-propyl ester

615250-74-3

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Basic information

Product Name: 2,2-Dimethyl-propionic acid (R)-3-((2R,4R,5S,6R)-5-acetoxy-4-dimethylamino-6-methyl-tetrahydro-pyran-2-yloxy)-2-(toluene-4-sulfonyloxy)-propyl ester
Synonyms:
CAS NO:615250-74-3
Molecular Formula:
Molecular Weight: 529.652
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: 2,2-Dimethyl-propionic acid (R)-3-((2R,4R,5S,6R)-5-acetoxy-4-dimethylamino-6-methyl-tetrahydro-pyran-2-yloxy)-2-(toluene-4-sulfonyloxy)-propyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2,2-Dimethyl-propionic acid (R)-3-((2R,4R,5S,6R)-5-acetoxy-4-dimethylamino-6-methyl-tetrahydro-pyran-2-yloxy)-2-(toluene-4-sulfonyloxy)-propyl ester(615250-74-3)
EPA Substance Registry System: 2,2-Dimethyl-propionic acid (R)-3-((2R,4R,5S,6R)-5-acetoxy-4-dimethylamino-6-methyl-tetrahydro-pyran-2-yloxy)-2-(toluene-4-sulfonyloxy)-propyl ester(615250-74-3)

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: 615250-74-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 615250-74-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,1,5,2,5 and 0 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 615250-74:
(8*6)+(7*1)+(6*5)+(5*2)+(4*5)+(3*0)+(2*7)+(1*4)=133
133 % 10 = 3
So 615250-74-3 is a valid CAS Registry Number.

615250-74-3Upstream product

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615250-74-3Relevant academic research and scientific papers

Glycidol-carbohydrate hybrids: A new family of DNA alkylating agents

Toshima, Kazunobu,Okuno, Yukiko,Matsumura, Shuichi

, p. 3281 - 3283 (2007/10/03)

Novel and chiral glycidol-carbohydrate hybrids possessing an epoxy group as a DNA alkylating moiety were designed and synthesized. These artificial hybrids selectively alkylated DNA at the N-7 sites of the guanines and cleaved DNA without any additives. The binding ability of the glycidol was significantly enhanced by the attachment of the carbohydrate.

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