tert-butyl beta-carboline-3-carboxylate

Names

[ CAS No. ]:
93835-05-3

[ Name ]:
tert-butyl beta-carboline-3-carboxylate

[Synonym ]:
MFCD06407911

Chemical & Physical Properties

[ Density]:
1.238g/cm3

[ Boiling Point ]:
470ºC at 760mmHg

[ Molecular Formula ]:
C₁₆H₁₆N₂O₂

[ Molecular Weight ]:
268.31000

[ Flash Point ]:
238.1ºC

[ Exact Mass ]:
268.12100

[ PSA ]:
54.98000

[ LogP ]:
3.67140

[ Index of Refraction ]:
1.661

MSDS

Safety Information

[ RIDADR ]:
NONH for all modes of transport

[ HS Code ]:
2933990090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

3-(imidazole)carbonyl-β-carboline
tert-Butanol
Lycoperodine 1
9H-pyrido[3,4-b]indole-3-carboxylic acid
DL-Tryptophan
ETHYL BETA-CARBOLINE-3-CARBOXYLATE
1,2,3,4-Tetrahydro-9H-pyrido[3,4-b]indol-3-carbonsaeureethylester
β-carboline-3-carboxylic acid chloride
Lithium tert-butoxide

DownStream

Customs

[ HS Code ]: 2933990090

[ Summary ]:
2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Articles

βCCT, an antagonist selective for α(1)GABA(A) receptors, reverses diazepam withdrawal-induced anxiety in rats.

Brain Res. Bull. 91 , 1-7, (2013)

The abrupt discontinuation of prolonged benzodiazepine treatment elicits a withdrawal syndrome with increased anxiety as a major symptom. The neural mechanisms underlying benzodiazepine physical depen...

Apparent pA2 values of benzodiazepine antagonists and partial agonists in monkeys.

J. Pharmacol. Exp. Ther. 290(3) , 1222-9, (1999)

Drugs that bind to benzodiazepine recognition sites of gamma-aminobutyric acid type A receptor complexes may function as agonists in some behavioral assays and as antagonists in other behavioral assay...

Cognition-impairing effects of benzodiazepine-type drugs: role of GABAA receptor subtypes in an executive function task in rhesus monkeys.

Pharmacol. Biochem. Behav. 104 , 62-8, (2013)

The present studies evaluated the role of α1 and α5 subunit-containing GABAA receptors (α1GABAA and α5GABAA receptors, respectively) in the ability of benzodiazepine (BZ)-type drugs to alter performan...

leucinamide-beta-carboline-3-carboxylate methyl ester
ETHYL BETA-CARBOLINE-3-CARBOXYLATE
METHYL 1-PHENYL-2,3,4,9-TETRAHYDRO-1H-BETA-CARBOLINE-3-CARBOXYLATE
Methyl (3R)-2-acetyl-2,3,4,9-tetrahydro-1H-beta-carboline-3-carboxylate
Methyl (3R)-2-(chloroacetyl)-2,3,4,9-tetrahydro-1H-beta-carboline-3-carboxylate
(tert-butyl)[beta-oxo-3,4-bis(p-toluoyloxy)phenethyl]ammonium trifluoroacetate
2-[2-[5-(Aminocarbonyl)-1-ethyl-1,6-dihydro-2-hydroxy-4-methyl-6-oxo-3-pyridinyl]diazenyl]-4-[[4-chloro-6-[[4-[[2-(sulfooxy)ethyl]sulfonyl]phenyl]amino]-1,3,5-triazin-2-yl]amino]benzenesulfonic acid
2-[2-[8-[[4-[[3-[[[2-(Ethenylsulfonyl)ethyl]amino]carbonyl]phenyl]amino]-6-fluoro-1,3,5-triazin-2-yl]amino]-1-hydroxy-3,6-disulfo-2-naphthalenyl]diazenyl]-1,5-naphthalenedisulfonic acid
4-(3-((2-Bromoprop-2-enoyl)amino)benzamido)-6-((5-((2-bromoprop-2-enoyl)amino)-2-sulfophenyl)diazenyl)-5-hydroxynaphthalene-1,7-disulfonic acid
2-[2-[8-[[4-Chloro-6-[[4-[[2-(sulfooxy)ethyl]sulfonyl]phenyl]amino]-1,3,5-triazin-2-yl]amino]-1-hydroxy-3,6-disulfo-2-naphthalenyl]diazenyl]-1,5-naphthalenedisulfonic acid
C.I. Reactive Red 227 parent
Reactive Red MS
3-Methoxy-3-methylbutanimidamide
1-[(5-Bromofuran-2-yl)methyl]cyclobutane-1-carbaldehyde
5-Iodo-7-methyl-2(1H)-quinoxalinone
1-(2H-Triazol-4-ylmethyl)cyclopentane-1-carboxylic acid;hydrochloride

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