15395
Boc-6-Ahx-OH
≥99.0% (T)
동의어(들):
6-(Boc-amino)caproic acid, 6-(Boc-amino)hexanoic acid, Boc-6-aminohexanoic acid
로그인조직 및 계약 가격 보기
모든 사진(1)
About This Item
Linear Formula:
(CH3)3CO2CNH(CH2)5CO2H
CAS Number:
Molecular Weight:
231.29
Beilstein:
2049561
MDL number:
UNSPSC 코드:
12352209
PubChem Substance ID:
NACRES:
NA.22
추천 제품
Quality Level
분석
≥99.0% (T)
양식
solid
반응 적합성
reaction type: Boc solid-phase peptide synthesis
mp
35-40 °C
응용 분야
peptide synthesis
저장 온도
2-8°C
SMILES string
CC(C)(C)OC(=O)NCCCCCC(O)=O
InChI
1S/C11H21NO4/c1-11(2,3)16-10(15)12-8-6-4-5-7-9(13)14/h4-8H2,1-3H3,(H,12,15)(H,13,14)
InChI key
RUFDYIJGNPVTAY-UHFFFAOYSA-N
유사한 제품을 찾으십니까? 방문 제품 비교 안내
기타 정보
Protected derivative to introduce the ε-aminocaproyl moiety in various compounds. Introduction of an aminocaproyl spacer arm in affinity chromatography.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
dust mask type N95 (US), Eyeshields, Gloves
이미 열람한 고객
A J Schroit et al.
Biochemistry, 22(15), 3617-3623 (1983-07-19)
An efficient method for the synthesis and purification of a variety of iodinated phospholipid analogues is described. 1-Acyl-2-[[[3-(3-[125I]iodo-4-hydroxyphenyl)- propionyl]amino]caproyl]phosphatidylcholine (125I-PC) was prepared by alkylation of 1-acyl-2-(aminocaproyl)phosphatidylcholine with monoiodinated Bolton-Hunter reagent. 125I-Labeled phosphatidic acid, phosphatidylethanolamine, and phosphatidylserine were produced from 125I-PC
J. Frank et al.
Helvetica Chimica Acta, 60, 2550-2550 (1977)
The literature on affinity chromatography.
M Wilchek et al.
Methods in enzymology, 34, 3-10 (1974-01-01)
Affinity chromatography of carboxypeptidase B.
M Sokolovsky
Methods in enzymology, 34, 411-414 (1974-01-01)
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