Cas 845522-46-5,(6-Fluoro-pyrido[3,4-d]pyrimidin-4-yl)-(trans-4-methyl-cyclohexyl)-amine

845522-46-5

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Basic information

Product Name: (6-Fluoro-pyrido[3,4-d]pyrimidin-4-yl)-(trans-4-methyl-cyclohexyl)-amine
Synonyms: (6-Fluoro-pyrido[3,4-d]pyrimidin-4-yl)-(trans-4-methyl-cyclohexyl)-amine
CAS NO:845522-46-5
Molecular Formula:
Molecular Weight: 260.314
EINECS: N/A
Product Categories: N/A
Mol File: 845522-46-5.mol
Article Data: 2

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: (6-Fluoro-pyrido[3,4-d]pyrimidin-4-yl)-(trans-4-methyl-cyclohexyl)-amine(CAS DataBase Reference)
NIST Chemistry Reference: (6-Fluoro-pyrido[3,4-d]pyrimidin-4-yl)-(trans-4-methyl-cyclohexyl)-amine(845522-46-5)
EPA Substance Registry System: (6-Fluoro-pyrido[3,4-d]pyrimidin-4-yl)-(trans-4-methyl-cyclohexyl)-amine(845522-46-5)

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: 845522-46-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 845522-46-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,5,5,2 and 2 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 845522-46:
(8*8)+(7*4)+(6*5)+(5*5)+(4*2)+(3*2)+(2*4)+(1*6)=175
175 % 10 = 5
So 845522-46-5 is a valid CAS Registry Number.

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845522-46-5Relevant articles and documents

Microwave-assisted synthesis of mGluR1 ligands: carbon, nitrogen and oxygen linked derivatives of pyrido[3,4-d]pyrimidin-4-ylamines

Harbottle, Gareth W.,Feeder, Neil,Gibson, Karl R.,Glossop, Mel,Maw, Graham N.,Million, William A.,Morel, Florence F.,Osborne, Simon,Poinsard, Cedric

, p. 4293 - 4296 (2008/02/12)

The syntheses of 6-fluoropyrido[3,4-d]pyrimidin-4-ylamine derivatives is reported herein. Methods for generating C, N and O linked analogues under microwave irradiation are described.

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