Cas 594860-66-9,4-carbamoyl-1-[2-O-acetyl-3-O-benzyl-5,6-dideoxy-6-(diethoxyphosphinyl)-6,6-difluoro-β-D-ribofuranosyl]-1,3-imidazolium-5-olate

594860-66-9

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Basic information

Product Name: 4-carbamoyl-1-[2-O-acetyl-3-O-benzyl-5,6-dideoxy-6-(diethoxyphosphinyl)-6,6-difluoro-β-D-ribofuranosyl]-1,3-imidazolium-5-olate
Synonyms:
CAS NO:594860-66-9
Molecular Formula:
Molecular Weight: 561.476
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: 4-carbamoyl-1-[2-O-acetyl-3-O-benzyl-5,6-dideoxy-6-(diethoxyphosphinyl)-6,6-difluoro-β-D-ribofuranosyl]-1,3-imidazolium-5-olate(CAS DataBase Reference)
NIST Chemistry Reference: 4-carbamoyl-1-[2-O-acetyl-3-O-benzyl-5,6-dideoxy-6-(diethoxyphosphinyl)-6,6-difluoro-β-D-ribofuranosyl]-1,3-imidazolium-5-olate(594860-66-9)
EPA Substance Registry System: 4-carbamoyl-1-[2-O-acetyl-3-O-benzyl-5,6-dideoxy-6-(diethoxyphosphinyl)-6,6-difluoro-β-D-ribofuranosyl]-1,3-imidazolium-5-olate(594860-66-9)

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: 594860-66-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 594860-66-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,9,4,8,6 and 0 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 594860-66:
(8*5)+(7*9)+(6*4)+(5*8)+(4*6)+(3*0)+(2*6)+(1*6)=209
209 % 10 = 9
So 594860-66-9 is a valid CAS Registry Number.

594860-66-9Upstream product

56973-26-3 5-hydroxy-1H-imidazole-4-carboxamide

594860-66-9Downstream Products

594860-66-9Relevant academic research and scientific papers

Synthesis of Azole Nucleoside 5′-Monophosphate Mimics (P1Ms) and Their Inhibitory Properties of IMP Dehydrogenases

Wang, Guangyi,Sakthivel, Kandasamy,Rajappan, Vasanthakumar,Bruice, Thomas W.,Tucker, Kathleen,Fagan, Patrick,Brooks, Jennifer L.,Hurd, Tiffany,Leeds, Janet M.,Cook, P. Dan

, p. 317 - 337 (2007/10/03)

IMPDH inhibitors have potential antimicrobial, anticancer and immunomodulatory effects. Nucleoside inhibitors of IMPDH exert their inhibitory effects via nucleoside 5′-MPs. Conversion of nucleoside analogs to NMPs by cellular nucleoside kinases is not ass

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