Cas 810683-45-5,4-Methylsulfanyl-6-[(E)-2-(2,6,6-trimethyl-cyclohex-1-enyl)-vinyl]-pyrimidin-2-ylamine

810683-45-5

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Basic information

Product Name: 4-Methylsulfanyl-6-[(E)-2-(2,6,6-trimethyl-cyclohex-1-enyl)-vinyl]-pyrimidin-2-ylamine
Synonyms: 4-Methylsulfanyl-6-[(E)-2-(2,6,6-trimethyl-cyclohex-1-enyl)-vinyl]-pyrimidin-2-ylamine
CAS NO:810683-45-5
Molecular Formula:
Molecular Weight: 289.445
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-Methylsulfanyl-6-[(E)-2-(2,6,6-trimethyl-cyclohex-1-enyl)-vinyl]-pyrimidin-2-ylamine(CAS DataBase Reference)
NIST Chemistry Reference: 4-Methylsulfanyl-6-[(E)-2-(2,6,6-trimethyl-cyclohex-1-enyl)-vinyl]-pyrimidin-2-ylamine(810683-45-5)
EPA Substance Registry System: 4-Methylsulfanyl-6-[(E)-2-(2,6,6-trimethyl-cyclohex-1-enyl)-vinyl]-pyrimidin-2-ylamine(810683-45-5)

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: 810683-45-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 810683-45-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,1,0,6,8 and 3 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 810683-45:
(8*8)+(7*1)+(6*0)+(5*6)+(4*8)+(3*3)+(2*4)+(1*5)=155
155 % 10 = 5
So 810683-45-5 is a valid CAS Registry Number.

810683-45-5Upstream product

50-01-1 guanidine hydrochloride

810683-45-5Downstream Products

952419-04-4 (CH₃)3C₆H₆CHCHC₄H₃N₃SO₂CH₃

810683-45-5Relevant academic research and scientific papers

Synthesis and antileishmanial profile of some novel terpenyl pyrimidines

Pandey, Susmita,Suryawanshi,Gupta, Suman,M.L. Srivastava

, p. 969 - 973 (2004)

Some novel terpenyl pyrimidine derivatives 2(a-d) and 6(a-b) have been synthesised from α/β-ionone keteneacetals 1 and 5. The terpenyl pyrimidine 2e has been synthesised from β-ionone 3 in two steps in quantitative yield. The pyrimidine derivatives were s

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