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3-(1-Methyl-4-piperidinyl)-1H-indol-5-ol structure, CAS 57477-39-1

3-(1-Methyl-4-piperidinyl)-1H-indol-5-ol

CAS Number57477-39-1

Synonyms5-hydroxy-3-(1-methylpiperidin-4-yl)indole; 3-(1-methyl-piperidin-4-yl)-indol-5-ol; 3-(1-Methylpiperidin-4-yl)-1H-indol-5-ol; BRL-54443; BRL 54443; Tocris-1129; 3-(1-Methyl-4-piperidinyl)-1H-indol-5-ol; Lopac-B-173; 3-(1-methylpiperidin-4-yl)1H-indol-5-ol

Molecular FormulaC14H18O1N2

Molecular Weight230.31

Purity98.00%

Density1.2±0.1 g/cm3

Boiling Point431.5±45.0 °C at 760 mmHg

Melting Point

Flash Point

Appearancesolid | white

EINECS

MSDSChineseEnglish

Symbol

Signal Word

Cat. No.: 2A-9044842 Purity: 98.00%
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Quality Control of [ 57477-39-1 ] Purity: 98.00% SDS Specification MoL

Chemical & Physical Properties
CAS Number57477-39-1
Catalog No.2A-9044842
Chinese Name3-(1-甲基-4-哌啶基)-1H-吲哚-5-醇
Synonyms5-hydroxy-3-(1-methylpiperidin-4-yl)indole; 3-(1-methyl-piperidin-4-yl)-indol-5-ol; 3-(1-Methylpiperidin-4-yl)-1H-indol-5-ol; BRL-54443; BRL 54443; Tocris-1129; 3-(1-Methyl-4-piperidinyl)-1H-indol-5-ol; Lopac-B-173; 3-(1-methylpiperidin-4-yl)1H-indol-5-ol
Molecular FormulaC14H18O1N2
Molecular Weight230.31
Purity98.00
Density1.2±0.1 g/cm3
Boiling Point431.5±45.0 °C at 760 mmHg
Appearancesolid | white
Water SolubilityH2O: 50 mg/mL
Storage Condition2-8°C
ApplicationBRL 54443 is a 5-HT1E/1F receptor agonist with pKi of 8.7 and 8.9 respectively. It is more than 30 times more inhibitory than other 5-HT and dopamine receptors.
HTC2933990090
PubChem ID5580999
MDL NumberMFCD01861184
SMILESCN1CCC(c2c[nH]c3ccc(O)cc23)CC1
InChIInChI=1S/C14H18N2O/c1-16-6-4-10(5-7-16)13-9-15-14-3-2-11(17)8-12(13)14/h2-3,8-10,15,17H,4-7H2,1H3
InChI KeyWKNFADCGOAHBPG-UHFFFAOYSA-N
MSDSmsds/44842_1_57477_39_1.pdf
Use ofProperties Name 3-(1-methylpiperidin-4-yl)-1H-indol-5-ol Synonym More Synonyms BRL-54443 Biological Activity Related Catalog Signaling Pathways >> GPCR/G Protein >> 5-HT Receptor Signaling Pathways >> Neuronal Signaling >> 5-HT Receptor Research Areas >> Cardiovascular Disease References [2]. McKune CM, et al. Characterization of the serotonin receptor mediating contraction in the mouse thoracic aorta and signal pathway coupling. J Pharmacol Exp Ther. 2001 Apr;297(1):88-95. [3]. Klein MT, et al. Distribution of 5-ht(1E) receptors in the mammalian brain and cerebral vasculature: an immunohistochemical and pharmacological study. Br J Pharmacol. 2012 Jun;166(4):1290-302. [4]. Granados-Soto V, et al. The role of peripheral 5-HT1A, 5-HT1B, 5-HT1D, 5-HT1E and 5-HT1F serotonergic receptors in the reduction of nociception in rats. Neuroscience. 2010 Jan 20;165(2):561-8. Chemical & Physical Properties Molecular Formula C14H18N2O Exact Mass 230.141907 PSA 39.26000 Appearance of Characters solid | white Index of Refraction 1.646 InChIKey WKNFADCGOAHBPG-UHFFFAOYSA-N Safety Information Hazard Codes Xi Safety Phrases 26-36 WGK Germany 3 HS Code 2933990090 Synthetic Route Total: 1 Page 5-METHOXY-3-(1-... CAS#:111963-87-2 CAS#:57477-39-1 Literature: Eli Lilly and Company Patent: US6358972 B1, 2002 ; US 6358972 B1 CAS#:1953-54-4 CAS#:57477-39-1 Literature: Medicinal Chemistry Research, , vol. 5, # 9 p. 680 - 689 Precursor & DownStream Precursor 2 CAS#:111963-87-2 5-METHOXY-3-(1-... CAS#:1953-54-4 DownStream 0
Tax Rebate13.0%
SupervisionNone. MFN tariff: 6.5%. Ordinary tariff: 20.0%
Transport InfoProduct name: 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%
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