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1H-Indole-1-carboxylic acid, 3-[[2,3,4,5-tetrahydro-1-[2-[(1-methylethyl)phenylamino]-2-oxoethyl]-2,4- dioxo-5-phenyl-1H-1,5-benzodiazepin-3-yl]methyl]-, 1,1-dimethylethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

174180-68-8

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174180-68-8 Usage

Molecular structure

The compound consists of an indole carboxylic acid core linked to a benzodiazepine ring system and a tert-butyl ester group.

Classification

It belongs to the class of benzodiazepines.

Pharmacological properties

Due to the presence of the benzodiazepine structure, the compound is likely to have sedative, anxiolytic, and muscle relaxant effects.

Specific substitution pattern

The specific substitution pattern on the benzodiazepine ring and the presence of the indole carboxylic acid moiety may contribute to the compound's biological activity and potential therapeutic applications.

Ester group

The presence of the tert-butyl ester group may affect the compound's pharmacokinetic properties, such as its solubility and stability.

Complexity

The compound is a complex molecule with multiple rings and functional groups, which may impact its chemical properties and potential applications.

Check Digit Verification of cas no

The CAS Registry Mumber 174180-68-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,4,1,8 and 0 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 174180-68:
(8*1)+(7*7)+(6*4)+(5*1)+(4*8)+(3*0)+(2*6)+(1*8)=138
138 % 10 = 8
So 174180-68-8 is a valid CAS Registry Number.

174180-68-8Downstream Products

174180-68-8Relevant academic research and scientific papers

CCK or gastrin modulating benzo ?b!?1,4! diazepines derivatives

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, (2008/06/13)

Benzo?b!?1,4!diazepine compounds of formula (I), where R1 is selected from C1 C6 alkyl, C3 -C6 cycloalkyl, phenyl, or substituted phenyl; R2 is selected from C3 -C6 alkyl, C3 C6 cycloalkyl, C3 -C6 alkenyl, benzyl, phenylC1 -C3 alkyl of substituted phenyl; or NR1 R2 together form 1,2,3,4-tetrahydroquinoline or benzazepine, mono-, di-, or trisubstituted independently with C1-6 alkyl C1-6 alkoxy or halogen substituents; p is an integer 0 or 1; q is an integer 0 or 1; r is an integer 0 or 1; t is an integer 0 or 1, provided that when r is 0 then t is 0; R3, R5, and R6 are independently hydrogen or C1-6 alkyl; R4 is C1-6 alkyl or C1-6 alkenyl; R7 is selected from the group consisting of hydrogen, C1-6 alkyl, C1-6 cycloalkyl, C1-6 alkenyl, phenyl, substituted phenyl, napthyl, heteroaryl, substituted heteroaryl, bicycloheteroaryl or substituted bicycloheteroaryl; or NR6 R7 together form a saturated 5,6, or 7 membered ring optionally interrupted by 1,2,3 or 4 N, S or O heteroatoms, with the proviso that any two O or S atoms are not bonded to each other, m is an integer selected from the group of 0, 1, 2, 3 or 4; R8 and R9 are selected from a variety of substituents; Z is hydrogen or halogen; novel intermediates, a pharmaceutical composition for treating obesity, gall bladder stasis, disorders of pancreatic secretion, methods for such treatment and processes for preparing compounds of formula (I).

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