673927
Ethyl N-Boc-4-methylpiperidine-4-carboxylate
97%
동의어(들):
1-tert-Butoxycarbonyl-4-methylpiperidine-4-carboxylic acid ethyl ester, 4-Methyl-1,4-piperidinedicarboxylic acid 1-(1,1-dimethylethyl) 4-ethyl ester
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모든 사진(1)
About This Item
실험식(Hill 표기법):
C14H25NO4
CAS Number:
Molecular Weight:
271.35
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22
추천 제품
분석
97%
refractive index
n20/D 1.4554
density
1.0134 g/mL at 25 °C
SMILES string
CCOC(=O)C1(C)CCN(CC1)C(=O)OC(C)(C)C
InChI
1S/C14H25NO4/c1-6-18-11(16)14(5)7-9-15(10-8-14)12(17)19-13(2,3)4/h6-10H2,1-5H3
InChI key
ZQZVWDXMUCTNRI-UHFFFAOYSA-N
애플리케이션
Reactant for synthesis of:
- Dipeptidyl peptidase-4 inhibitor ABT-279
- Building blocks for piperazine-based CCR5 antagonists
Replacement of the ester function with an amino group provides a key building block for piperazine-based CCR5 antagonists.[1]
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 3 Oral - Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3
표적 기관
Respiratory system
Storage Class Code
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 3
Flash Point (°F)
>230.0 °F
Flash Point (°C)
> 110 °C
개인 보호 장비
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Xiao-Hua Jiang et al.
Bioorganic & medicinal chemistry letters, 14(14), 3675-3678 (2004-06-19)
4-Substituted-4-aminopiperidine is an interesting structural motif found in a number of bioactive compounds. An efficient and convenient method for the synthesis of 4-differently substituted-4-aminopiperidine derivatives was described, employing isonipecotate as a starting material and Curtius rearrangement as a key step.
활성 필터
자사의 과학자팀은 생명 과학, 재료 과학, 화학 합성, 크로마토그래피, 분석 및 기타 많은 영역을 포함한 모든 과학 분야에 경험이 있습니다..
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