Cas 106689-01-4,(methyl-4 phenyl)-1 (methyl-4 benzoylamino)-3 (methyl-4 benzoylhydrazono)-4 tetrahydro-1,2,3,4 quinazoline

106689-01-4

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Basic information

Product Name: (methyl-4 phenyl)-1 (methyl-4 benzoylamino)-3 (methyl-4 benzoylhydrazono)-4 tetrahydro-1,2,3,4 quinazoline
Synonyms:
CAS NO:106689-01-4
Molecular Formula:
Molecular Weight: 503.604
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: (methyl-4 phenyl)-1 (methyl-4 benzoylamino)-3 (methyl-4 benzoylhydrazono)-4 tetrahydro-1,2,3,4 quinazoline(CAS DataBase Reference)
NIST Chemistry Reference: (methyl-4 phenyl)-1 (methyl-4 benzoylamino)-3 (methyl-4 benzoylhydrazono)-4 tetrahydro-1,2,3,4 quinazoline(106689-01-4)
EPA Substance Registry System: (methyl-4 phenyl)-1 (methyl-4 benzoylamino)-3 (methyl-4 benzoylhydrazono)-4 tetrahydro-1,2,3,4 quinazoline(106689-01-4)

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: 106689-01-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 106689-01-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,6,8 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 106689-01:
(8*1)+(7*0)+(6*6)+(5*6)+(4*8)+(3*9)+(2*0)+(1*1)=134
134 % 10 = 4
So 106689-01-4 is a valid CAS Registry Number.

106689-01-4Upstream product

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106689-01-4Relevant academic research and scientific papers

Composes sulfures heterocycliques CIV. Participation de groupe voisin dans des reactions des dihydro-1,2 benzothiazine-3,1 thiones-4

Legrand, Louis,Lozac'h, Noel

, p. 859 - 864 (2007/10/02)

A comparison of the reactions between amines or hydrazines with 1-alkyl- (or 1-aryl-) 1,2-dihydro-3,1-benzothiazine-4-thiones 1 shows the influence as well of the latter's substituents in position 1 (alkyl or aryl) as of the nature of the nucleophilic rea

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