252808
Octyl chloroformate
97%
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About This Item
Linear Formula:
ClCO2(CH2)7CH3
CAS Number:
Molecular Weight:
192.68
UNSPSC Code:
12352100
PubChem Substance ID:
EC Number:
231-224-9
MDL number:
InChI key
VFXVAXFIFHSGNR-UHFFFAOYSA-N
InChI
1S/C9H17ClO2/c1-2-3-4-5-6-7-8-12-9(10)11/h2-8H2,1H3
SMILES string
CCCCCCCCOC(Cl)=O
vapor pressure
0.39 psi ( 20 °C)
assay
97%
form
liquid
refractive index
n20/D 1.431 (lit.)
bp
90-91 °C/11 mmHg (lit.)
density
0.984 g/mL at 25 °C (lit.)
storage temp.
2-8°C
Application
Octyl chloroformate has been used in preparation of:
- octyl 4-[(tetrahydropyran-2-yl)oxy]but-2-ynoate
- octyl 4-methoxybut-2-ynoate
- octyl 4,4-diethoxybut-2-ynoate
- N-octyloxycarbonyl-R110
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Oral - Skin Corr. 1B
Storage Class
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
wgk
WGK 3
flash_point_f
168.8 °F - closed cup
flash_point_c
76 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Regulatory Information
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Regio-and enantioselective synthesis of allenic esters by samarium (II)-mediated reduction of propargylic compounds through dynamic kinetic protonation.
Mikami K and Yoshida A.
Tetrahedron, 57(5), 889-898 (2001)
S X Cai et al.
Bioorganic & medicinal chemistry letters, 11(1), 39-42 (2001-01-05)
N-Octyloxycarbonyl-R110 (1), with enhanced cell penetration and retention properties, was prepared from rhodamine 110. The tetrapeptide substrate N-Ac-DEVD-N'-octyloxycarbonyl-R110 (3) was prepared and shown to be efficiently cleaved by human recombinant caspase-3 and by apoptotic HL-60 cells. This substrate should prove
Tomáš Hložek et al.
Journal of analytical toxicology, 40(9), 749-753 (2016-09-04)
A simple, sensitive and robust method for simultaneous determination of antiepileptic drugs (gabapentin, pregabalin and vigabatrin) in human serum using GC-MS was developed and validated for clinical toxicology purposes. This method employs an emerging class of derivatization agents - alkyl
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