T13005
1,2,3,4-四氢异喹啉
95%
别名:
1,2,3,4-四氢-2-异喹啉, 1,2,3,4-四氢-2-氮杂萘, 1,2,3,4-四氢异喹啉, 3,4-二氢-1H-异喹啉
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关于此项目
经验公式（希尔记法）:
C9H11N
化学文摘社编号:
分子量:
133.19
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-050-0
Beilstein/REAXYS Number:
116156
MDL number:
Assay:
95%
Quality Level
assay
95%
refractive index
n20/D 1.568 (lit.)
bp
232-233 °C (lit.)
mp
−30 °C (lit.)
density
1.064 g/mL at 25 °C (lit.)
SMILES string
C1Cc2ccccc2CN1
InChI
1S/C9H11N/c1-2-4-9-7-10-6-5-8(9)3-1/h1-4,10H,5-7H2
InChI key
UWYZHKAOTLEWKK-UHFFFAOYSA-N
Gene Information
human ... PNMT(5409)
rat ... Adra2a(25083), Htr1a(24473)
signalword
Danger
Hazard Classifications
Acute Tox. 2 Dermal - Acute Tox. 3 Oral - Acute Tox. 4 Inhalation - Aquatic Chronic 3 - Eye Dam. 1 - Skin Corr. 1B - STOT SE 2
存储类别
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
wgk
WGK 3
flash_point_f
210.2 °F - closed cup
flash_point_c
99 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
Man-Ho So et al.
Chemistry, an Asian journal, 4(10), 1551-1561 (2009-09-25)
Selective oxidation of amines using oxygen as terminal oxidant is an important area in green chemistry. In this work, we describe the use of graphite-supported gold nanoparticles (AuNPs/C) to catalyze aerobic oxidation of cyclic and acyclic benzylic amines to the
Suvankar Banerjee et al.
Journal of biomolecular structure & dynamics, 38(5), 1551-1564 (2019-05-11)
Histone deacetylase 8 (HDAC8) is one of the crucial HDACs responsible for influencing the epigenetic functions of the body. Overexpression of HDAC8 is found to be involved in numerous disease conditions such as tumorigenesis, cell proliferation, cancer, viral infections, neuronal
Gustavo P Romanelli et al.
Molecular diversity, 14(4), 803-807 (2009-07-03)
The preparation of N-sulfonyl-1,2,3,4-tetrahydroisoquinolines, N-sulfonyl-2,3,4,5-tetrahydro-1H-2-benzazepines and N-sulfonyl-1,2,3,4,5,6-hexahydrobenzazocine was catalyzed by a Preyssler heteropolyacid, H(14)[NaP(5)W(30)O(110)], (PA), supported on silica (PASiO(2)40) with excellent yields by means of the Pictet-Spengler reaction of N-aralkylsulfonamides with s-trioxane. The reactions proceed with 0.5 mol% of silica-supported
Gary L Grunewald et al.
Bioorganic & medicinal chemistry, 15(3), 1298-1310 (2006-11-28)
1,2,3,4-Tetrahydrobenz[h]isoquinoline (THBQ, 11) is a potent, inhibitor of phenylethanolamine N-methyltransferase (PNMT). Docking studies indicated that the enhanced PNMT inhibitory potency of 11 (hPNMT K(i)=0.49microM) versus 1,2,3,4-tetrahydroisoquinoline (5, hPNMT K(i)=5.8microM) was likely due to hydrophobic interactions with Val53, Met258, Val272, and
Matthias Ludwig et al.
European journal of medicinal chemistry, 41(8), 1003-1010 (2006-05-06)
A series of 1-aryl-1,2,3,4-tetrahydroisoquinoline and 8-methyl-1-aryl-1,2,3,4-tetrahydroisoquinoline derivatives was evaluated for affinity to the PCP binding site of the NMDA receptor complex. The (S)-configured tetrahydroisoquinoline derivative (S)-4 e x HCl bearing a 2-methylphenyl substituent in position 1 of the heterocyclic ring
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| T13005-25G | 04061837337086 |
| T13005-100G | 04061837337079 |
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