91308-65-5 Usage
Uses
Used in Pharmaceutical Applications:
1-(2-furyl)-1,2,3,4-tetrahydro-9H-pyrido(3,4-b)indole-3-carboxylic acid is used as a potential pharmaceutical agent for [application reason] due to its unique molecular structure and potential biological activity. 1-(2-furyl)-1,2,3,4-tetrahydro-9H-pyrido(3,4-b)indole-3-carboxylic acid's furan ring and tetrahydro-9H-pyrido(3,4-b)indole core, along with the carboxylic acid group, may contribute to its effectiveness in [specific therapeutic area or mechanism of action].
Used in Research and Development:
In the field of chemical research and development, 1-(2-furyl)-1,2,3,4-tetrahydro-9H-pyrido(3,4-b)indole-3-carboxylic acid serves as a valuable compound for [application type] because of [application reason]. Its complex structure and potential reactivity with other molecules make it an interesting candidate for exploring new chemical reactions or as a starting material for the synthesis of novel compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 91308-65-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,3,0 and 8 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 91308-65:
(7*9)+(6*1)+(5*3)+(4*0)+(3*8)+(2*6)+(1*5)=125
125 % 10 = 5
So 91308-65-5 is a valid CAS Registry Number.
InChI:InChI=1/C16H14N2O3/c19-16(20)12-8-10-9-4-1-2-5-11(9)17-14(10)15(18-12)13-6-3-7-21-13/h1-7,12,15,17-18H,8H2,(H,19,20)/t12-,15-/m0/s1
91308-65-5Relevant academic research and scientific papers
Isolation and identification of 1-furyl-β-carboline derivatives that are mutagenic after nitrite treatment
Kanamori,Kinae,Saito,Tomita
, p. 1980 - 1986 (2007/10/02)
When a mixture of 2-furaldehyde (I) and L-tryptophan dissolved in 0.1 M phosphate buffer (pH 7.0) was kept at 37°C for 4 weeks, a browning reaction gradually occurred. The reaction mixture after treatment with nitrite at pH 4.0, was mutagenic to S. typhimurium TA100 in the absence of S9 mix. The browning solution was fractionated by applying high-performance liquid chromatography (HPLC) and thin-layer chromatography (TLC), and two 1-furyl-β-carboline derivatives were isolated. They were compound A, (1R,3S)-1-(2-furyl)-1,2,3,4-tetrahydro-9H-pyrido[3,4-b]indole-3-carboxylic acid, and compound B, (1S,3S)-1-(2-furyl)-1,2,3,4-tetrahydro-9H-pyrido[3,4-b]indole-3-carboxylic acid. These compounds had similar mutagenic potency toward S. typhimurium TA100 without metabolic actvity after treatment wih nitrite.
