Cas 1304501-75-4,4-methoxy-N2-(4-methoxyphenyl)-N1,N2-dipropylbenzene-1,2-diamine

1304501-75-4

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Basic information

Product Name: 4-methoxy-N₂-(4-methoxyphenyl)-N₁,N₂-dipropylbenzene-1,2-diamine
Synonyms: 4-methoxy-N₂-(4-methoxyphenyl)-N₁,N₂-dipropylbenzene-1,2-diamine
CAS NO:1304501-75-4
Molecular Formula:
Molecular Weight: 328.455
EINECS: N/A
Product Categories: N/A
Mol File: 1304501-75-4.mol
Article Data: 1

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-methoxy-N₂-(4-methoxyphenyl)-N₁,N₂-dipropylbenzene-1,2-diamine(CAS DataBase Reference)
NIST Chemistry Reference: 4-methoxy-N₂-(4-methoxyphenyl)-N₁,N₂-dipropylbenzene-1,2-diamine(1304501-75-4)
EPA Substance Registry System: 4-methoxy-N₂-(4-methoxyphenyl)-N₁,N₂-dipropylbenzene-1,2-diamine(1304501-75-4)

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: 1304501-75-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1304501-75-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,0,4,5,0 and 1 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1304501-75:
(9*1)+(8*3)+(7*0)+(6*4)+(5*5)+(4*0)+(3*1)+(2*7)+(1*5)=104
104 % 10 = 4
So 1304501-75-4 is a valid CAS Registry Number.

1304501-75-4Upstream product

71193-47-0 N-(4-methoxyphenyl)-N-propylamine

1304501-75-4Downstream Products

1304501-75-4Relevant articles and documents

A dehydrogenative homocoupling reaction for the direct synthesis of hydrazines from N-alkylanilines in air

Yan, Xue-Ming,Chen, Zhi-Ming,Yang, Fei,Huang, Zhi-Zhen

supporting information; experimental part, p. 569 - 572 (2011/04/22)

A copper-catalyzed N-N bond-forming reaction was performed by a dehydrogenative homocoupling of N-alkylanilines, affording N,N-dialkyl-N,N- diphenylhydrazines in 72-88% yields. This new strategy has the advantages of direct synthesis from N-alkylanilines,

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