601-01-4 Usage
Description
ALLOTETRAHYDRO S, also known as tetrahydro-2H-pyran-4-ylidenamine, is a chemical compound that serves as a versatile intermediate in organic synthesis. It is composed of a tetrahydro-2H-pyran-4-ylidenamine active ingredient, which makes it a valuable building block in the synthesis of complex organic compounds. Its ability to act as a reagent in organic synthesis and its applications in the pharmaceutical and chemical industries highlight its importance in the field of organic chemistry.
Uses
Used in Pharmaceutical Industry:
ALLOTETRAHYDRO S is used as a versatile intermediate for the preparation of various nitrogen-containing molecules, which are essential in the development of pharmaceutical compounds. Its unique structure allows for the creation of a wide range of nitrogen-containing organic molecules, making it a valuable asset in the synthesis of new drugs and therapeutic agents.
Used in Chemical Industry:
In the chemical industry, ALLOTETRAHYDRO S is utilized as a reagent in organic synthesis, contributing to the production of heterocyclic compounds and other complex organic molecules. Its role as a building block in the synthesis of complex organic compounds makes it an important chemical in the development of various chemical products and materials.
Used in Organic Synthesis:
ALLOTETRAHYDRO S is used as a reagent in organic synthesis for the preparation of a variety of nitrogen-containing molecules. Its unique structure and properties make it an ideal candidate for the synthesis of complex organic compounds, which can be further used in various applications across different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 601-01-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,0 and 1 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 601-01:
(5*6)+(4*0)+(3*1)+(2*0)+(1*1)=34
34 % 10 = 4
So 601-01-4 is a valid CAS Registry Number.
601-01-4Relevant articles and documents
A convenient synthesis of the side chain of loteprednol etabonate - An ocular soft corticosteroid from 20-oxopregnanes using metal-mediated halogenation as a key reaction
Chowdhury, Pritish,Borah, Juri Moni,Goswami, Papori,Das, Archana Moni
experimental part, p. 497 - 501 (2011/05/09)
A facile synthesis of the side chain of loteprednol etabonate, namely, chloromethyl-17α-[(ethoxycarbonyl))oxy]-11β-hydro of loteprednol etabonate, viz., chloromethyl-17α-[(ethoxycarbonyl))oxy]-11xy-3- oxoandrosta-1,4-diene-17β-carboxylate - an ocular soft corticosteroid, has been described starting from a 20-oxopregnane, namely, 3β-acetoxy-pregn- 5(6),16(17)-diene-20-one (16-dehydropregnenolone acetate, i.e., 16-DPA) using our recently developed metal-mediated halogenation as a key reaction.
Biotransformation of corticosteroids by Penicillium decumbens ATCC 10436
Holland, Herbert L.
, p. 646 - 649 (2007/10/02)
The biotransformation of a series of corticosteroids by the fungus Penicillium decumbens ATCC 10436 has been investigated. Conversion to the corresponding 5α-dihydroxteroid was observed for all the Δ4-3-ketosteroids studied with the exception of deoxycorticosterone, which was converted to a Δ14-diene. Deoxycorticosterone acetate was, however, converted to a 5α- dihydro product concomitant with ester hydrolysis. Other substrates carrying a C-21 acetoxy group were also hydrolyzed to the alcohol. In two cases (resulting from deoxycorticosterone acetate and 11-deoxycortisone) the 5α- 3-keto-product was further reduced to the 3β-alcohol. No reduction of δ14-dienes was observed.
Chemical conversion of corticosteroids to 3α,5α-tetrahydro derivatives. Synthesis of allotetrahydro-11-deoxycortisol glucuronides
Hosoda,Takasaki,Miura,et al.
, p. 4281 - 4287 (2007/10/02)
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