104270-87-3 Usage
Description
Benzoic acid, 6-formyl-2,3-dimethoxy-, ethyl ester is an organic compound that serves as an intermediate in the synthesis of various chemical compounds. It is characterized by the presence of a benzene ring with a formyl group at the 6-position and two methoxy groups at the 2 and 3 positions, as well as an ethyl ester group.
Uses
Used in Pharmaceutical Industry:
Benzoic acid, 6-formyl-2,3-dimethoxy-, ethyl ester is used as an intermediate in the synthesis of (+/-)-β-Hydrastine (H675690), which is an inhibitor of dopamine biosynthesis. This makes it a valuable compound in the development of medications targeting dopamine-related disorders.
Used in Chemical Synthesis:
Benzoic acid, 6-formyl-2,3-dimethoxy-, ethyl ester can also be used as a starting material or intermediate in the synthesis of other organic compounds, particularly those with potential applications in various industries such as pharmaceuticals, agrochemicals, and materials science. Its unique structure allows for further functionalization and modification to create new molecules with specific properties and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 104270-87-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,2,7 and 0 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 104270-87:
(8*1)+(7*0)+(6*4)+(5*2)+(4*7)+(3*0)+(2*8)+(1*7)=93
93 % 10 = 3
So 104270-87-3 is a valid CAS Registry Number.
104270-87-3Relevant articles and documents
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Wegscheider
, p. 311 (1893)
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First Rational Synthesis of the Thiothiono Analogue of an Unsymmetrically Substituted Phthalic Anhydride
Morrison, Christopher F.,Burnell, D. Jean
, p. 3891 - 3892 (2007/10/03)
equation presented Treatment of the dithiolane derivative of an α-carboxyethyl benzaldehyde with LDA at -78°C smoothly produced the thiothionophthalic anhydride. The mechanism is proposed to involve loss of ethene and attack of an intermediate dithiocarboxylate onto the ester. Heating the thiothionophthalic anhydride gave the 3,3′-bithiophthalide.
