Cas 140244-53-7,2-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-N-(2-methoxyphenyl)-3-methylbutanamide

140244-53-7

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Basic information

Product Name: 2-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-N-(2-methoxyphenyl)-3-methylbutanamide
Synonyms: 2-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-N-(2-methoxyphenyl)-3-methylbutanamide
CAS NO:140244-53-7
Molecular Formula: C₂₀H₂₀N₂O₄
Molecular Weight: 352.3838
EINECS: N/A
Product Categories: N/A
Mol File: 140244-53-7.mol
Article Data: 1

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 2-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-N-(2-methoxyphenyl)-3-methylbutanamide(CAS DataBase Reference)
NIST Chemistry Reference: 2-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-N-(2-methoxyphenyl)-3-methylbutanamide(140244-53-7)
EPA Substance Registry System: 2-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-N-(2-methoxyphenyl)-3-methylbutanamide(140244-53-7)

Safety Data

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 140244-53-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 140244-53-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,0,2,4 and 4 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 140244-53:
(8*1)+(7*4)+(6*0)+(5*2)+(4*4)+(3*4)+(2*5)+(1*3)=87
87 % 10 = 7
So 140244-53-7 is a valid CAS Registry Number.

140244-53-7Upstream product

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140244-53-7Relevant articles and documents

SYNTHESIS AND REACTIONS OF PHTHALIMIDO ALIPHATIC ACID AZIDES

Essawy, Samy A.,El-Aleem, A. H. Abd,Donia, S. G.,Metwally, R. N.

, p. 1243 - 1250 (2007/10/02)

Azides (2a-d), in the base catalyzed decomposition with aromatic amines yielded the corresponding N-aryl-N'-alkyl ureas (4a-t) via Curtius rearrangement.However, the base catalyzed decomposition of 2 with phenylhydrazine took place via azido group displacement to afford phthalimido aliphatic acid phenylhydrazides (8a-d).Decomposition of azides (2a-d) in neutral medium yielded the corresponding sym-N,N'-di-alkyl ureas (9a-d), via Curtius rearrangement.

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