Cas 164797-59-5,Furo[3,4-b]furan-3-carboxylic acid, 4,6-dihydro- (9CI)

164797-59-5

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Basic information

Product Name: Furo[3,4-b]furan-3-carboxylic acid, 4,6-dihydro- (9CI)
Synonyms: Furo[3,4-b]furan-3-carboxylic acid, 4,6-dihydro- (9CI)
CAS NO:164797-59-5
Molecular Formula: C7H6O4
Molecular Weight: 154.12014
EINECS: N/A
Product Categories: CARBOXYLICACID
Mol File: 164797-59-5.mol

Chemical Properties

Melting Point: N/A
Boiling Point: 329.3±42.0 °C(Predicted)
Flash Point: N/A
Appearance: /
Density: 1.469±0.06 g/cm3(Predicted)
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
PKA: 4.12±0.20(Predicted)
CAS DataBase Reference: Furo[3,4-b]furan-3-carboxylic acid, 4,6-dihydro- (9CI)(CAS DataBase Reference)
NIST Chemistry Reference: Furo[3,4-b]furan-3-carboxylic acid, 4,6-dihydro- (9CI)(164797-59-5)
EPA Substance Registry System: Furo[3,4-b]furan-3-carboxylic acid, 4,6-dihydro- (9CI)(164797-59-5)

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: 164797-59-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 164797-59-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,4,7,9 and 7 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 164797-59:
(8*1)+(7*6)+(6*4)+(5*7)+(4*9)+(3*7)+(2*5)+(1*9)=185
185 % 10 = 5
So 164797-59-5 is a valid CAS Registry Number.

164797-59-5Upstream product

107710-62-3 methyl 4,6-dihydrofuro<3,4-b>furan-3-carboxylate

164797-59-5Downstream Products

164797-59-5Relevant academic research and scientific papers

A,B-Diheteropentalenes by a Tandem Intramolecular Diels-Alder/Reverse Diels-Alder Reaction Sequence. Application to the Synthesis of Thienofuran

Buttery, Jarrod H.,Moursounidis, John,Wege, Dieter

, p. 593 - 608 (1995)

Alkylation of 2-furylmethanethiol (28) with propargyl chloride gave the thioether (22) which on methoxycarbonylation afforded the acetylenic ester (30).On heating, this material underwent an intramolecular Diels-Alder reaction to give the tricyclic compou

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