N-tert-부톡시카르보닐-1,6-헥산디아민

한글명:N-tert-부톡시카르보닐-1,6-헥산디아민

카스 번호51857-17-1

상품명:N-BOC-1,6-diaminohexane

CBNumberCB0702254

분자식C11H24N2O2

포뮬러 무게216.32

MOL 파일51857-17-1.mol

동의어(한글)

N-tert-부톡시카르보닐-1,6-헥산디아민

화학적 성질

끓는 점	106-110 °C (0.3 mmHg)
밀도	0.965 g/mL at 20 °C(lit.)
굴절률	n20/D 1.462
인화점	125 °C
저장 조건	Keep in dark place,Inert atmosphere,2-8°C
용해도	디클로로메탄과 에틸 아세테이트에 용해됩니다.
산도 계수 (pKa)	12.93±0.46(Predicted)
물리적 상태	점성 액체
색상	맑은 연한 노란색
감도	Air Sensitive
BRN	2089264
InChIKey	RVZPDKXEHIRFPM-UHFFFAOYSA-N
CAS 데이터베이스	51857-17-1(CAS DataBase Reference)

위험 및 안전 성명

위험품 표기

위험 카페고리 넘버

안전지침서

26-36/37/39-45

유엔번호(UN No.)

UN 2735 8/PG 2

WGK 독일

F 고인화성물질

10-34

위험 등급

포장분류

III

HS 번호

29241900

NFPA 704:

	1
3		1

그림문자(GHS)

N-tert-부톡시카르보닐-1,6-헥산디아민 화학적 특성, 용도, 생산

화학적 성질
Off-White Solid
용도
N-Boc-1,6-diaminohexane is used to prepare 1,3-Bis[6-(Boc-amino)hexyl]urea by reacting with carbonyl dichloride in the presence of triethylamine. Further, it is used as a reagent for the introduction of a C6-spacer.
주요 응용
N-Boc-1,6-hexanediamine can be used as a linear hexyl spacer (C6-spacer) to synthesize:
Biodegradable poly(disulfide amine)s for gene delivery.
A multifunctional dendrimer for theranostics.
Polyamide platinum anti-cancer complexes designed to target cancer specific DNA sequences.
Self-assembled monolayers (SAMs) that resist adsorption of proteins.
[N-(6-(4-Hydroxy-6-isopropylamino-1,3,5-triazin-2-ylamino)hexyl)-5-hydroxy-1,4-naphthoquinone-3-propionamide] (JUG-HATZ), which can be used in designing electrochemical immunosensors.
제조 방법
synthesis of N-BOC-1,6-diaminohexane: 1,6-Diaminohexane 3 (Fig. 1) (100 g, 0.86 mol) was dissolved in CH2Cl2 (300 ml) and cooled in an ice bath to 0–3°C. To the stirred solution 0.3 eq. di-tert-butyl bicarbonate (62.6 g, 0.29 mol) was added slowly over a period of 1 h. The reaction was allowed to warm up to r.t., and proceeded overnight. The reaction mixture was extracted with saturated aqueous NaHCO3 (50 ml, three times). The organic phases were pooled, dried, and evaporated under reduced pressure. The resulting oil was dissolved in 200 ml, 1 N HCl and extracted with ether. The aqueous phase was washed with ether, made basic to a pH of 10 with aqueous 2 N NaO3, and extracted with ethyl acetate. The organic phases were pooled, dried, and evaporated under reduced pressure. The resulting oil was dissolved in 200 ml, 1 N HCL and extracted with ether. The aqueous phase was washed with ether, made basic to a pH of 10 with aqueous 2 N NaOH, and extracted with ethyl acetate. The organic extracts were pooled, dried over Na2SO4 and evaporated to give 10.5 g of homogeneous N-BOC-1, 6- diaminohexane 2c (Fig. 1) as a yellow oil which was used without further purification.
TLC Rf 0.51; 1H NMR (CDCL3) d 4.54 (bs, 1H; NH), 3.05 1 2.62 (m, 4H; NCH2), 1.41 (m, 9H; CH3), 1.29 (m, 8H; CH2).
Evaluation of aminoalkylmethacrylate nanoparticles as colloidal drug carrier systems. Part I: synthesis of monomers, dependence of the physical properties on the polymerization methods

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