N-1-나프탈레닐-1,2-에테인다이아민

N-(1-Naphthyl)ethylenediamine

HCID 15107

노트 반응

부분 구조 검색 유사 구조 찾기

기본 정보

CAS: 551-09-7
표준 SMILES: NCCNc1cccc2ccccc12
InChIKey: NULAJYZBOLVQPQ-UHFFFAOYSA-N
분자식: C12H14N2
평균 분자량: 186.25 g/mol
단동위원소 질량: 186.11569846

이름 및 식별자

우선 이름: N-(1-Naphthyl)ethylenediamine
IUPAC: N'-naphthalen-1-ylethane-1,2-diamine
현지명: N-1-나프탈레닐-1,2-에테인다이아민
영어명: N-(1-naphthyl)ethylenediamine
분자식: C12H14N2
분자량: 186.25

이름 및 동의어

N-(1-Naphthyl)ethylenediamine551-09-7N-(1-naphthyl)ethane-1,2-diamineN-1-naphthylethylenediamine02X37521XEDTXSID7043744CHEBI:53510RefChem:823647N-1-EDANN-1-ethylenediaminonaphthaleneDTXCID5023744208-992-9

이름 더 보기

N-1-나프탈레닐-1,2-에테인다이아민naphthylethylenediamine1-NAPHTHYLETHYLENEDIAMINEN-(1-Naphtyl)ethylenediamineN-(1-Naphtyl)ethane-1,2-diamineN-(1-Naphtyl)-1,2-ethanediamineN-1-NAPHTHALENYL-1,2-ETHANEDIAMINE)N1-1-Naphthalenyl-1,2-ethanediamine1,2-Ethanediamine, N1-1-naphthalenyl-

N1-(naphthalen-1-yl)ethane-1,2-diamineN-(naphthalen-1-yl)ethane-1,2-diamine1,2-Ethanediamine, N-1-naphthalenyl-N'-naphthalen-1-ylethane-1,2-diamineCHEMBL1214195N'-(1-naphthyl)ethane-1,2-diamineNCGC00163705-03Oprea1_329986

데이터베이스 식별자

CAS: 551-09-7
PubChem CID: 15107
DTXSID: DTXSID7043744
ChEMBL: CHEMBL1214195
ChEBI: CHEBI:53510
UNII: 02X37521XE
EC Number: 208-992-9
Nikkaji: J60.112H

물성

구조 계산 물성

XLogP: 1.9
극성 표면적: 38.1 Å²
수소 결합 공여자 수: 2
수소 결합 수용자 수: 2
회전 가능 결합 수: 3
무거운 원자 수: 14
형식 전하: 0
복잡도: 170

실험 및 물리화학적 성질

Physical DescriptionStraw-yellow viscous liquid; [Merck Index]

물리화학적 성질

녹는점: 229 · 229.0-231.6 °C(Solv: dichloromethane (75-09-2))
끓는 점: 9 · bp9 204°; bp760 ~320° (dec)
밀도: 425 · d425 1.114
굴절률: 25 · nD25 1.6648
산도 계수 (pKa): 9.43 · 9.43±0.10(Predicted)
EPA: 1 · 1,2-Ethanediamine, N-1-naphthalenyl- (551-09-7)

안전 및 규제

유해성 정보

Hazards SummarySee N-(1-Naphthyl)ethylenediamine dihydrochloride.

안전 데이터

tsca: TSCA listed
기존화학 물질: KE-25591

화학 및 산업

용도 및 제조

General Manufacturing Information1,2-Ethanediamine, N1-1-naphthalenyl-: ACTIVE

응용 분야 · 1건

용도N-(Naphthalen-1-yl)ethane-1,2-diamine can be used in the preparation, cytotoxicity study and SAR of N-benzylpiperidine carboxamide derivatives as potential cholinesterase inhibitors for treatment of Alzheimer''s disease. It can be used in the preparation of iminodiethoxy cyclotriphosphazene derivatives with potential antimicrobial activities. It can also be useful in biophysical screens to identify fragments that bind to the viral DNA-binding proteins EBNA1 and LANA.