Cas 1244546-98-2,(Z)-(2,6-dimethylphenyl)-(3-heptyl-4-methylmorpholin-2-ylidene)amine

1244546-98-2

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Basic information

Product Name: (Z)-(2,6-dimethylphenyl)-(3-heptyl-4-methylmorpholin-2-ylidene)amine
Synonyms: (Z)-(2,6-dimethylphenyl)-(3-heptyl-4-methylmorpholin-2-ylidene)amine
CAS NO:1244546-98-2
Molecular Formula:
Molecular Weight: 302.46
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: (Z)-(2,6-dimethylphenyl)-(3-heptyl-4-methylmorpholin-2-ylidene)amine(CAS DataBase Reference)
NIST Chemistry Reference: (Z)-(2,6-dimethylphenyl)-(3-heptyl-4-methylmorpholin-2-ylidene)amine(1244546-98-2)
EPA Substance Registry System: (Z)-(2,6-dimethylphenyl)-(3-heptyl-4-methylmorpholin-2-ylidene)amine(1244546-98-2)

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: 1244546-98-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1244546-98-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,4,5,4 and 6 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1244546-98:
(9*1)+(8*2)+(7*4)+(6*4)+(5*5)+(4*4)+(3*6)+(2*9)+(1*8)=162
162 % 10 = 2
So 1244546-98-2 is a valid CAS Registry Number.

1244546-98-2Upstream product

1244546-98-2Downstream Products

1244546-98-2Relevant academic research and scientific papers

Isocyanide based multicomponent reactions of oxazolidines and related systems

Waller, Robert W.,Diorazio, Louis J.,Taylor, Brian A.,Motherwell, William B.,Sheppard, Tom D.

experimental part, p. 6496 - 6507 (2010/10/03)

N-Alkyloxazolidines react in a multicomponent reaction with carboxylic acids and isocyanides to give N-acyloxyethylamino acid amides. The previously reported reaction conditions were improved using a design of experiments approach (DoE). Under the optimis

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