Cas 188897-45-2,Carbamic acid, [1-(3,4-dimethoxyphenyl)-2-fluorocyclopropyl]-, 1,1-dimethylethyl ester

188897-45-2

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Basic information

Product Name: Carbamic acid, [1-(3,4-dimethoxyphenyl)-2-fluorocyclopropyl]-, 1,1-dimethylethyl ester
Synonyms:
CAS NO:188897-45-2
Molecular Formula: C16H22FNO4
Molecular Weight: 311.353
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: Carbamic acid, [1-(3,4-dimethoxyphenyl)-2-fluorocyclopropyl]-, 1,1-dimethylethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Carbamic acid, [1-(3,4-dimethoxyphenyl)-2-fluorocyclopropyl]-, 1,1-dimethylethyl ester(188897-45-2)
EPA Substance Registry System: Carbamic acid, [1-(3,4-dimethoxyphenyl)-2-fluorocyclopropyl]-, 1,1-dimethylethyl ester(188897-45-2)

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: 188897-45-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 188897-45-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,8,8,9 and 7 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 188897-45:
(8*1)+(7*8)+(6*8)+(5*8)+(4*9)+(3*7)+(2*4)+(1*5)=222
222 % 10 = 2
So 188897-45-2 is a valid CAS Registry Number.

188897-45-2Upstream product

188897-45-2Downstream Products

188897-45-2Relevant academic research and scientific papers

Synthesis of a fluorinated analog of 1-aminocyclopropane carboxylic acid

Sloan, Milton J.,Kirk, Kenneth L.

, p. 1677 - 1680 (2007/10/03)

A convenient synthesis of 2-fluoro-1-aminocyclopropane-1-carboxylic acid is described. Cyclopropanation of ethyl 2-(3,4-dimethoxyphenyl)-3-fluoroacrylate followed by Curtius rearrangement, oxidative cleavage of the aromatic ring, and deprotection, produced the α-amino acid.

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