Cas 90344-83-5,2,4-Diazabicyclo[3.2.0]heptane-1-carboxylic acid, 2,4,6,6-tetramethyl-3-oxo-

90344-83-5

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Basic information

Product Name: 2,4-Diazabicyclo[3.2.0]heptane-1-carboxylic acid, 2,4,6,6-tetramethyl-3-oxo-
Synonyms:
CAS NO:90344-83-5
Molecular Formula: C10H16N2O3
Molecular Weight: 212.249
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: 2,4-Diazabicyclo[3.2.0]heptane-1-carboxylic acid, 2,4,6,6-tetramethyl-3-oxo-(CAS DataBase Reference)
NIST Chemistry Reference: 2,4-Diazabicyclo[3.2.0]heptane-1-carboxylic acid, 2,4,6,6-tetramethyl-3-oxo-(90344-83-5)
EPA Substance Registry System: 2,4-Diazabicyclo[3.2.0]heptane-1-carboxylic acid, 2,4,6,6-tetramethyl-3-oxo-(90344-83-5)

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: 90344-83-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 90344-83-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,3,4 and 4 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 90344-83:
(7*9)+(6*0)+(5*3)+(4*4)+(3*4)+(2*8)+(1*3)=125
125 % 10 = 5
So 90344-83-5 is a valid CAS Registry Number.

90344-83-5Upstream product

90296-02-9 cis-6-fluoro-2,4,8,8-tetramethyl-2,4-diazabicyclo<4.2.0>octane-3,5-dione

90344-83-5Downstream Products

90344-83-5Relevant academic research and scientific papers

A Novel Mechanism for Conversion of 5-Fluorouracil-Olefin Photocycloaddition Products to 5-Substituted Uracils. A Synthon for the Uracil 5-Carbanion

Wexler, Allan J.,Balchunis, Robert J.,Swenton, John S.,Kaminski, Victor V.

, p. 2738 - 2743 (1984)

The photocycloaddition products of 5-fluorouracil and enol acetates undergo fragmentation reactions to afford 5-substituted uracils in good yields.Unexpectedly, certain 5-fluorouracil-olefin photocycloaddition products react with 3 equiv of potassium tert

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