96087
N-苄氧羰基-1,6-二氨基己烷 盐酸盐
≥97% (AT)
别名:
N-(6-氨基己基)氨基甲酸苄酯 盐酸盐, N-Z-1,6-二氨基己烷 盐酸盐
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关于此项目
线性分子式:
C6H5CH2OCONH(CH2)6NH2 · HCl
化学文摘社编号:
分子量:
286.80
UNSPSC Code:
12352200
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
4727129
Assay:
≥97% (AT)
Form:
crystals
InChI
1S/C14H22N2O2.ClH/c15-10-6-1-2-7-11-16-14(17)18-12-13-8-4-3-5-9-13;/h3-5,8-9H,1-2,6-7,10-12,15H2,(H,16,17);1H
SMILES string
Cl[H].NCCCCCCNC(=O)OCc1ccccc1
InChI key
GMSZGOGHNFZOMF-UHFFFAOYSA-N
assay
≥97% (AT)
form
crystals
reaction suitability
reagent type: cross-linking reagent
mp
175-180 °C
Other Notes
引入六亚甲基二胺连接基
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
此项目有
M M Ponpipom et al.
Carbohydrate research, 113(1), 45-56 (1983-02-16)
Spacer arms 2.1-3.7 nm (21-37 A) long were prepared, and coupled with the methyl beta-glycoside of N-acetylmuramyl-L-alanyl-D-isoglutamine benzyl ester, to give blocked 6-acylates. Deprotection was effected with palladium chloride and triethyl-silane. Chemical conjugates of MDP-meningococcal group C polysaccharide were then
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