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1-(6-aminobenzo[d][1,3]dioxol-5-yl)ethanol is a chemical compound characterized by its molecular formula C10H11NO3. It features a six-membered aromatic ring fused with a dioxole ring and an amino group, classifying it as an ethanol derivative with a hydroxyl group attached to a two-carbon chain. This versatile compound is known for its potential biological activities and pharmacological properties, making it a promising candidate for drug development and synthesis in the pharmaceutical industry.

927833-63-4

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927833-63-4 Usage

Uses

Used in Pharmaceutical Industry:
1-(6-aminobenzo[d][1,3]dioxol-5-yl)ethanol is used as a building block for the synthesis of various drugs and medications. Its unique structure and potential biological activities contribute to its value in creating new and effective pharmaceutical compounds.
Used in Drug Development:
1-(6-aminobenzo[d][1,3]dioxol-5-yl)ethanol is utilized as a versatile component in drug development due to its potential pharmacological properties. Its precise applications are still under investigation, but the compound's structure and characteristics make it a promising candidate for creating innovative and effective medications.

Check Digit Verification of cas no

The CAS Registry Mumber 927833-63-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,7,8,3 and 3 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 927833-63:
(8*9)+(7*2)+(6*7)+(5*8)+(4*3)+(3*3)+(2*6)+(1*3)=204
204 % 10 = 4
So 927833-63-4 is a valid CAS Registry Number.

927833-63-4Downstream Products

927833-63-4Relevant academic research and scientific papers

Synthesis of the antitumoural agent batracylin and related isoindolo[1,2-b]quinazolin-12(10H)-ones

Martínez-Viturro, Carlos M.,Domínguez, Domingo

, p. 1023 - 1026 (2008/02/04)

The synthesis of batracylin and related isoindolo[1,2-b]quinazolin-12-ones from easily accessible o-acylanilines is reported. The preparation of these tetracyclic compounds through a Mitsunobu reaction followed by spontaneous cyclodehydration shows the ability of this methodology to afford good yields of a wide variety of diversely 7, 8, 9, 10-substituted isoindoloquinazolinones in two steps.

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