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Carbonochloridic acid,octyl ester

Names

[ CAS No. ]:
7452-59-7

[ Name ]:
Carbonochloridic acid,octyl ester

[Synonym ]:
octyl carbonochloridate
MFCD00000652
EINECS 231-224-9

Chemical & Physical Properties

[ Density]:
0.984

[ Boiling Point ]:
90-91ºC (11 mmHg)

[ Molecular Formula ]:
C9H17ClO2

[ Molecular Weight ]:
192.68300

[ Flash Point ]:
75ºC

[ Exact Mass ]:
192.09200

[ PSA ]:
26.30000

[ LogP ]:
3.72230

[ Appearance of Characters ]:
Liquid | Clear colorless

[ Index of Refraction ]:
1.43-1.432

[ Storage condition ]:
0-6°C

MSDS

Safety Information

[ Symbol ]:

GHS05, GHS06

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H301 + H311 + H331-H314

[ Precautionary Statements ]:
P261-P280-P301 + P310-P305 + P351 + P338-P310

[ Personal Protective Equipment ]:
Faceshields;full-face respirator (US);Gloves;Goggles;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ Hazard Codes ]:
T

[ Risk Phrases ]:
34-23-23/24/25

[ Safety Phrases ]:
45-36/37/39-26-27

[ RIDADR ]:
UN 2742

[ Packaging Group ]:
II

[ Hazard Class ]:
6.1(a)

[ HS Code ]:
2915900090

Precursor & DownStream

Customs

[ HS Code ]: 2915900090

[ Summary ]:
2915900090 other saturated acyclic monocarboxylic acids and their anhydrides, halides, peroxides and peroxyacids; their halogenated, sulphonated, nitrated or nitrosated derivatives VAT:17.0% Tax rebate rate:9.0% Supervision conditions:AB(certificate of inspection for goods inward,certificate of inspection for goods outward) MFN tariff:5.5% General tariff:30.0%

Articles

Design and synthesis of rhodamine 110 derivative and caspase-3 substrate for enzyme and cell-based fluorescent assay.

Bioorg. Med. Chem. Lett. 11(1) , 39-42, (2001)

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 an...

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) , 889-98, (2001)


More Articles


Related Compounds

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