Cas 78664-29-6,4-<(3-chloro-2-quinoxalinyl)azo>-5-chloro-3-methyl-1-phenylpyrazole

78664-29-6

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Basic information

Product Name: 4-<(3-chloro-2-quinoxalinyl)azo>-5-chloro-3-methyl-1-phenylpyrazole
Synonyms:
CAS NO:78664-29-6
Molecular Formula:
Molecular Weight: 383.239
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-<(3-chloro-2-quinoxalinyl)azo>-5-chloro-3-methyl-1-phenylpyrazole(CAS DataBase Reference)
NIST Chemistry Reference: 4-<(3-chloro-2-quinoxalinyl)azo>-5-chloro-3-methyl-1-phenylpyrazole(78664-29-6)
EPA Substance Registry System: 4-<(3-chloro-2-quinoxalinyl)azo>-5-chloro-3-methyl-1-phenylpyrazole(78664-29-6)

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: 78664-29-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 78664-29-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,6,6 and 4 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 78664-29:
(7*7)+(6*8)+(5*6)+(4*6)+(3*4)+(2*2)+(1*9)=176
176 % 10 = 6
So 78664-29-6 is a valid CAS Registry Number.

78664-29-6Upstream product

78664-28-5 (Z)-2,4-dihydro-5-methyl-2-phenyl-3H-pyrazole-3,4-dione 4-(3-chloro-2-quinoxalinyl)hydrazone

78664-29-6Downstream Products

78664-29-6Relevant academic research and scientific papers

Synthesis of macroheterocyclic compounds on the basis of 3-chloro-2-hydrazinoquinoxaline

Dziomko,Stopnikova,Shmelev,Ryabokobylko,Adamova,Gurevich,Poponova

, p. 401 - 406 (1981)

2-Amino-1-[(3-chloro-2-quinoxalinyl)azo]naphthalene was obtained by oxidative coupling of 3-chloro-2-hydrazinoquinoxaline with 2-aminonaphthalenesulfonic acid; cross self-cyclization of the product was used to synthesize macrocyclic compounds, viz., [1,2,

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