105949-40-4 Usage
Indole class
1-diethylcarbamoyl-3-formylindole belongs to the class of organic compounds known as indoles, which are derivatives of the benzofused bicyclic structure with a pyrrole ring.
Carbamoylindole derivative
This chemical compound is a derivative of carbamoylindole, meaning it has a similar structure to carbamoylindole but with modifications in its functional groups or side chains.
Yellow crystalline solid
The physical appearance of 1-diethylcarbamoyl-3-formylindole is a yellow crystalline solid, indicating its form and color.
Intermediate in synthesis
The compound is typically used as an intermediate in the synthesis of various pharmaceutical compounds and research chemicals, meaning it is a reactant in the production of other chemicals.
Potential cytotoxic and antitumor properties
1-diethylcarbamoyl-3-formylindole has been studied for its possible ability to inhibit cell growth (cytotoxic) and its potential to combat cancer (antitumor).
Production of dyes and pigments
This chemical is also used in the manufacturing of certain dyes and pigments, suggesting its application in the colorants industry.
Check Digit Verification of cas no
The CAS Registry Mumber 105949-40-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,9,4 and 9 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 105949-40:
(8*1)+(7*0)+(6*5)+(5*9)+(4*4)+(3*9)+(2*4)+(1*0)=134
134 % 10 = 4
So 105949-40-4 is a valid CAS Registry Number.
105949-40-4Relevant articles and documents
Benzothiazinone and benzoxazinone compounds
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Page/Page column 111, (2010/11/30)
Q is —N=or CR2 X is S, O or NOR3 Y is —O—, —S—, —SO— or —SO2— R and R1 are each, independently, H, a substituted or unsubstituted aliphatic, aromatic, heteroaromatic or aralkyl group R2 is H or a su
SYNTHESIS OF 3-SUBSTITUTED INDOLES VIA N-ACYLINDOLIUM IONS
Comins, Daniel L.,Stroud, Eric D.
, p. 1869 - 1872 (2007/10/02)
3-Substituted N-(N'N'-diethylcarbamyl)indoles are prepared from indole-3-carboxaldehyde in good overall yield via N-acylindolium ion intermediates.
