5-Tetralinylamine

1-NAPHTHALENAMINE, 5,6,7,8-TETRAHYDRO- · 5-Tetralylamine · 5-AMINOTETRALIN · Tetralin-5-amine · AKOS BBS-00003705 · 5-Tetralinylamine · TIMTEC-BB SBB004091 · 5,6,7,8-Tetrahydro-1

https://huagongshe.com/ko/chemical/16671

식별자 및 물리적 특성

CAS No.	2217-41-6
분자식	C10H13N
평균 분자량	147.22 g/mol
단동위원소 질량	147.10479942 g/mol
SMILES	Nc1cccc2c1CCCC2
InChIKey	SODWJACROGQSMM-UHFFFAOYSA-N
PubChem CID	16671
EC No.	218-713-2
DTXSID	DTXSID70176701

화학 및 물리적 성질

XLogP	2.6
극성 표면적	26
수소 결합 공여자 수	1
수소 결합 수용자 수	1
회전 가능 결합 수	0
무거운 원자 수	11
형식 전하	0
복잡도	133
SpringerMaterials Properties	Viscosity
녹는점	38 °C(lit.)
끓는 점	275-277 °C713 mm Hg(lit.)
밀도	1,06 g/cm3
굴절률	n20/D 1.590(lit.)
인화점	>230 °F
용해도	miscible with Alcohol
물리적 상태	액체
pKa(산도 계수)	4.56±0.20(Predicted)
색상	투명한 노란색에서 갈색까지
BRN	387264
InChI	1S/C10H13N/c11-10-7-3-5-8-4-1-2-6-9(8)10/h3,5,7H,1-2,4,6,11H2
InChIKey	SODWJACROGQSMM-UHFFFAOYSA-N
SMILES	Nc1cccc2CCCCc12
NIST	1-Naphthalenamine, 5,6,7,8-tetrahydro-(2217-41-6)

화학적 성질

Clear yellow to brown liquid

안전 및 규제

GHS 분류	WarningH315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)Aggregated GHS information provided per 41 reports by companies from 4 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
규제 정보	Chemical: 1-Naphthalenamine, 5,6,7,8-tetrahydro-1-Naphthalenamine, 5,6,7,8-tetrahydro-: Does not have an individual approval but may be used as a component in a product covered by a group standard. It is not approved for use as a chemical in its own right.
Hazard Classes and Categories	Skin Irrit. 2 (100%)
수질 위해 등급(WGK)	3
RTECS 번호	QM4780000
관세 코드	29214990
위험 문구(R)	36/37/38
위험 표시	Xi
안전 문구(S)	26-36
F 고인화성물질	9
저장 분류	10 - Combustible liquids

용도

5,6,7,8-Tetrahydro-1-naphthylamine is used as a reagent in the synthesis of GoSlo-SR-5-69, a potent activator of large conductance Ca2+-activated K+ (BK) channels. 5,6,7,8-Tetrahydro-1-naphthylamine is also used as a reagent in the synthesis of benzopyrans and related compounds as inhibitors of the hypoxia inducible factor pathway.