Cas 1355336-33-2,diethyl (E)-2-{[(2,4-dinitrophenyl)acetyl (tert-butylamino)]carbonyl}-2-butenedioate

1355336-33-2

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Basic information

Product Name: diethyl (E)-2-{[(2,4-dinitrophenyl)acetyl (tert-butylamino)]carbonyl}-2-butenedioate
Synonyms:
CAS NO:1355336-33-2
Molecular Formula:
Molecular Weight: 479.444
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: diethyl (E)-2-{[(2,4-dinitrophenyl)acetyl (tert-butylamino)]carbonyl}-2-butenedioate(CAS DataBase Reference)
NIST Chemistry Reference: diethyl (E)-2-{[(2,4-dinitrophenyl)acetyl (tert-butylamino)]carbonyl}-2-butenedioate(1355336-33-2)
EPA Substance Registry System: diethyl (E)-2-{[(2,4-dinitrophenyl)acetyl (tert-butylamino)]carbonyl}-2-butenedioate(1355336-33-2)

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: 1355336-33-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1355336-33-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,5,3,3 and 6 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1355336-33:
(9*1)+(8*3)+(7*5)+(6*5)+(5*3)+(4*3)+(3*6)+(2*3)+(1*3)=152
152 % 10 = 2
So 1355336-33-2 is a valid CAS Registry Number.

1355336-33-2Upstream product

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1355336-33-2Relevant academic research and scientific papers

Three-component reaction between alkyl isocyanides, dialkyl acetylenedicarboxylates, and carboxylic acids

Hassanabadi, Alireza,Mosslemin, Mohammad H.,Singh, Sonia,Shaterchi, Seyyed Ali

, p. 661 - 663,3 (2020/07/30)

Protonation of the reactive intermediates produced in the reaction between alkyl isocyanides and dialkyl acetylenedicarboxylates by carboxylic acids leads to vinylnitrilium cations which then undergo nucleophilic addition of the conjugate bases of the car

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