Cas 95250-05-8,ethyl 6,7-dichloro-2,3-dihydro-5-<3,5-bis<(dimethylamino)methyl>-4-hydroxybenzoyl>-2-benzofurancarboxylate dihydrochloride

95250-05-8

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Basic information

Product Name: ethyl 6,7-dichloro-2,3-dihydro-5-<3,5-bis<(dimethylamino)methyl>-4-hydroxybenzoyl>-2-benzofurancarboxylate dihydrochloride
Synonyms:
CAS NO:95250-05-8
Molecular Formula:
Molecular Weight: 568.325
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: ethyl 6,7-dichloro-2,3-dihydro-5-<3,5-bis<(dimethylamino)methyl>-4-hydroxybenzoyl>-2-benzofurancarboxylate dihydrochloride(CAS DataBase Reference)
NIST Chemistry Reference: ethyl 6,7-dichloro-2,3-dihydro-5-<3,5-bis<(dimethylamino)methyl>-4-hydroxybenzoyl>-2-benzofurancarboxylate dihydrochloride(95250-05-8)
EPA Substance Registry System: ethyl 6,7-dichloro-2,3-dihydro-5-<3,5-bis<(dimethylamino)methyl>-4-hydroxybenzoyl>-2-benzofurancarboxylate dihydrochloride(95250-05-8)

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: 95250-05-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 95250-05-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,2,5 and 0 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 95250-05:
(7*9)+(6*5)+(5*2)+(4*5)+(3*0)+(2*0)+(1*5)=128
128 % 10 = 8
So 95250-05-8 is a valid CAS Registry Number.

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95250-05-8Relevant academic research and scientific papers

[(Aminomethyl)aryloxy]acetic acid esters. A new class of high-ceiling diuretics. 4. Substituted 6,7-dichloro-2,3-dihydrobenzofurans derived by ring annelation.

Lee,Parks,Bunnell,Plattner,Field,Giebisch

, p. 589 - 594 (2007/10/02)

Ring annelation of the [(aminomethyl)aryloxy]acetic acids produced a series of substituted 6,7-dichloro-2,3-dihydrobenzofuran-2-carboxylic acids. Pharmacologic evaluation of these compounds in rats and dogs indicated that several congeners are extremely p

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