Cas 42775-87-1,2-[(3aR,5S,6S,6aR)-5-(2,2-Dimethyl-[1,3]dioxolan-4-yl)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-yl]-isoindole-1,3-dione

42775-87-1

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Basic information

Product Name: 2-[(3aR,5S,6S,6aR)-5-(2,2-Dimethyl-[1,3]dioxolan-4-yl)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-yl]-isoindole-1,3-dione
Synonyms:
CAS NO:42775-87-1
Molecular Formula:
Molecular Weight: 389.405
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: 2-[(3aR,5S,6S,6aR)-5-(2,2-Dimethyl-[1,3]dioxolan-4-yl)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-yl]-isoindole-1,3-dione(CAS DataBase Reference)
NIST Chemistry Reference: 2-[(3aR,5S,6S,6aR)-5-(2,2-Dimethyl-[1,3]dioxolan-4-yl)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-yl]-isoindole-1,3-dione(42775-87-1)
EPA Substance Registry System: 2-[(3aR,5S,6S,6aR)-5-(2,2-Dimethyl-[1,3]dioxolan-4-yl)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-yl]-isoindole-1,3-dione(42775-87-1)

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: 42775-87-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 42775-87-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,7,7 and 5 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 42775-87:
(7*4)+(6*2)+(5*7)+(4*7)+(3*5)+(2*8)+(1*7)=141
141 % 10 = 1
So 42775-87-1 is a valid CAS Registry Number.

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42775-87-1Relevant academic research and scientific papers

NEW SYNTHETIC "TRICKS". ONE-POT PREPARATION OF N-SUBSTITUTED PHTHALIMIDES FROM AZIDES AND PHTHALIC ANHYDRIDE

Garcia, Jordi,Vilarrasa, Jaume,Bordas, Xavier,Banaszek, Anna

, p. 639 - 640 (2007/10/02)

N-Substituted phthalimides can be obtained in very good yields, under essentially neutral conditions, by mixing or heating an alkyl (or aryl) azide, triphenylphosohine, and phthalic anhydride in benzene or toluene, in the presence of a catalytic amount of tetrabutylammonium cyanide.Application of the reaction into the domain of carbohydrates is promising.

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