416444
3-(Boc-amino)-1-propanol
97%
Synonym(s):
tert-Butyl N-(3-hydroxypropyl)carbamate
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About This Item
Linear Formula:
(CH3)3COC(O)NHCH2CH2CH2OH
CAS Number:
Molecular Weight:
175.23
Beilstein:
1860807
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
97%
form
liquid
reaction suitability
reagent type: cross-linking reagent
refractive index
n20/D 1.453
density
1.025 g/mL at 20 °C (lit.)
functional group
Boc
amine
hydroxyl
SMILES string
OCCCNC(OC(C)(C)C)=O
InChI
1S/C8H17NO3/c1-8(2,3)12-7(11)9-5-4-6-10/h10H,4-6H2,1-3H3,(H,9,11)
InChI key
XDJCYKMWJCYQJM-UHFFFAOYSA-N
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Application
Amine protected, difunctional reagent employed in the synthesis of phosphatidyl ethanolamines and ornithine.
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point(F)
228.2 °F - closed cup
Flash Point(C)
109 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Synthesis, 133-133 (1993)
Synthetic Communications, 21, 359-359 (1991)
Lan Yao et al.
Polymers, 12(5) (2020-05-28)
Polymeric nanomaterials made from amphiphilic block copolymers are increasingly used in the treatment of tumor tissues. In this work, we firstly synthesized the amphiphilic block copolymer PBnMA-b-P(BAPMA-co-PEGMA) via reversible addition-fragmentation chain transfer (RAFT) polymerization using benzyl methacrylate (BnMA), poly (ethylene
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 416444-50ML | 4061838127396 |
| 416444-10ML | 4061838054081 |
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