Cas 847414-99-7,1H-Pyrazolo[3,4-d]pyrimidin-4-amine, N-[trans-4-[(2R)-2-fluoro-2-(2-fluorophenyl)ethoxy]cyclohexyl]-

847414-99-7

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Basic information

Product Name: 1H-Pyrazolo[3,4-d]pyrimidin-4-amine, N-[trans-4-[(2R)-2-fluoro-2-(2-fluorophenyl)ethoxy]cyclohexyl]-
Synonyms:
CAS NO:847414-99-7
Molecular Formula: C19H21F2N5O
Molecular Weight: 373.405
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: 1H-Pyrazolo[3,4-d]pyrimidin-4-amine, N-[trans-4-[(2R)-2-fluoro-2-(2-fluorophenyl)ethoxy]cyclohexyl]-(CAS DataBase Reference)
NIST Chemistry Reference: 1H-Pyrazolo[3,4-d]pyrimidin-4-amine, N-[trans-4-[(2R)-2-fluoro-2-(2-fluorophenyl)ethoxy]cyclohexyl]-(847414-99-7)
EPA Substance Registry System: 1H-Pyrazolo[3,4-d]pyrimidin-4-amine, N-[trans-4-[(2R)-2-fluoro-2-(2-fluorophenyl)ethoxy]cyclohexyl]-(847414-99-7)

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: 847414-99-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 847414-99-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,7,4,1 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 847414-99:
(8*8)+(7*4)+(6*7)+(5*4)+(4*1)+(3*4)+(2*9)+(1*9)=197
197 % 10 = 7
So 847414-99-7 is a valid CAS Registry Number.

847414-99-7Upstream product

847414-99-7Downstream Products

847414-99-7Relevant academic research and scientific papers

An efficient synthesis of an NMDA receptor antagonist via stereoselective fluorination

Bio, Matthew M.,Waters, Marjorie,Javadi, Gary,Song, Zhiguo Jake,Zhang, Fei,Thomas, Dave

, p. 891 - 896 (2008)

Herein is described the development and use of a novel bis(dialkylamino) sulfur difluoride reagent to effect the stereoselective conversion of a benzylic alcohol into a benzylic fluoride. A new method for the synthesis of 1H-pyrazolo[3,4-d]pyrimidin-4-ami

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