Cas 1319736-42-9,methyl 4-(hydroxyimino)-5-{[2-(hydroxyimino)-3-phenylpropyl][2-(hydroxyimino)propyl]amino}pentanoate

1319736-42-9

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Basic information

Product Name: methyl 4-(hydroxyimino)-5-{[2-(hydroxyimino)-3-phenylpropyl][2-(hydroxyimino)propyl]amino}pentanoate
Synonyms:
CAS NO:1319736-42-9
Molecular Formula:
Molecular Weight: 378.428
EINECS: N/A
Product Categories: N/A
Mol File: 1319736-42-9.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: methyl 4-(hydroxyimino)-5-{[2-(hydroxyimino)-3-phenylpropyl][2-(hydroxyimino)propyl]amino}pentanoate(CAS DataBase Reference)
NIST Chemistry Reference: methyl 4-(hydroxyimino)-5-{[2-(hydroxyimino)-3-phenylpropyl][2-(hydroxyimino)propyl]amino}pentanoate(1319736-42-9)
EPA Substance Registry System: methyl 4-(hydroxyimino)-5-{[2-(hydroxyimino)-3-phenylpropyl][2-(hydroxyimino)propyl]amino}pentanoate(1319736-42-9)

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: 1319736-42-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1319736-42-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,9,7,3 and 6 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1319736-42:
(9*1)+(8*3)+(7*1)+(6*9)+(5*7)+(4*3)+(3*6)+(2*4)+(1*2)=169
169 % 10 = 9
So 1319736-42-9 is a valid CAS Registry Number.

1319736-42-9Upstream product

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1319736-42-9Relevant articles and documents

A general procedure for the synthesis of unsymmetrically substituted tris(β-oximinoalkyl)amines

Semakin, Artem N.,Sukhorukov, Alexey Yu.,Ioffe, Sema L.,Tartakovsky, Vladimir A.

experimental part, p. 1403 - 1412 (2011/06/19)

A first general approach to the synthesis of unsymmetrically substituted tris(β-oximinoalkyl)amines containing two or three different β-oximinoalkyl fragments has been developed. This procedure employs available aliphatic nitro compounds as starting build

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