252808
Octyl chloroformate
97%
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About This Item
Linear Formula:
ClCO2(CH2)7CH3
CAS Number:
Molecular Weight:
192.68
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
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
SMILES string
CCCCCCCCOC(Cl)=O
InChI
1S/C9H17ClO2/c1-2-3-4-5-6-7-8-12-9(10)11/h2-8H2,1H3
InChI key
VFXVAXFIFHSGNR-UHFFFAOYSA-N
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
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 3 Oral - Skin Corr. 1B
Storage Class Code
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
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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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
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)
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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