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Merck

668796

Sigma-Aldrich

(S)-(+)-1,2,3,4-四氢-1-萘胺

97%

别名:

(S)-(+)-1-AminoTetralin, (S)-(+)-1-氨基四氢化萘

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About This Item

线性分子式:
(C10H11)NH2
CAS号:
分子量:
147.22
Beilstein:
2360279
MDL號碼:
分類程式碼代碼:
12352116
PubChem物質ID:
NACRES:
NA.22

化驗

97%

折射率

n20/D 1.565

bp

250 °C

密度

1.010 g/mL at 25 °C

SMILES 字串

N[C@H]1CCCc2ccccc12

InChI

1S/C10H13N/c11-10-7-3-5-8-4-1-2-6-9(8)10/h1-2,4,6,10H,3,5,7,11H2/t10-/m0/s1

InChI 密鑰

JRZGPXSSNPTNMA-JTQLQIEISA-N

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應用

(S)-(+)-1,2,3,4-Tetrahydro-1-naphthylamine is a chiral amine that can be used:
  • To prepare a 2-pyridylmethylene-(S)-(+)-1,2,3,4-tetrahydro-1-naphthylamine containing pentanuclear trigonal bipyramidal [Co3Fe2] complex, which exhibits electron-transfer-coupled spin transition (ETCST) properties.
  • To prepare imine-substituted thiophene Schiff base compounds.
  • To derivatize macrocyclic diarylheptanoid compounds of biological importance.

法律資訊

象形圖

CorrosionExclamation mark

訊號詞

Danger

危險聲明

危險分類

Acute Tox. 4 Oral - Aquatic Chronic 3 - Skin Corr. 1C

儲存類別代碼

8A - Combustible corrosive hazardous materials

水污染物質分類(WGK)

WGK 3

個人防護裝備

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter


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其他客户在看

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Synthesis and antibacterial evaluation of macrocyclic diarylheptanoid derivatives
Lin H, et al.
Bioorganic & medicinal chemistry letters, 26(16), 4070-4076 (2016)
Crystal structures of four chiral imine-substituted thiophene derivatives
Hern'andez-T'ellez G, et al.
Acta Crystallographica Section E: Crystallographic Communications, 72(3), 350-354 (2016)
Solvent-induced on/off switching of intramolecular electron transfer in a cyanide-bridged trigonal bipyramidal complex
Wei R-J, et al.
Dalton Transactions, 45(43), 17104-17107 (2016)

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