4-METHOXYPHENYLACETYL CHLORIDE

[ Density]:
1.208 g/mL at 25 °C(lit.)

[ Boiling Point ]:
143 °C10 mm Hg(lit.)

[ Molecular Formula ]:
C₉H₉ClO₂

[ Molecular Weight ]:
184.62000

[ Flash Point ]:
>230 °F

[ Exact Mass ]:
184.02900

[ PSA ]:
26.30000

[ LogP ]:
2.00310

[ Index of Refraction ]:
n20/D 1.54(lit.)

[ Storage condition ]:
2-8°C

Click to get detail MSDS

[ Symbol ]:

GHS05

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H314

[ Supplemental HS ]:
Reacts violently with water.

[ Precautionary Statements ]:
P280-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 ]:
C:Corrosive;

[ Risk Phrases ]:
R34

[ Safety Phrases ]:
S26-S36/37/39-S45

[ RIDADR ]:
UN 3265 8/PG 2

[ WGK Germany ]:
3

[ Packaging Group ]:
II

[ Hazard Class ]:
8

Click to get detail synthetic route

Synthesis of substituted spiro [4.5] deca-3, 6, 9-triene-2, 8-diones: an expeditious route to the spiro [4.5] decane terpene skeleton. Haack RA and Beck KR.

Tetrahedron Lett. 30(13) , 16505-8, (1989)

Synthesis of higenamine, A cardiotonic principle of aconite root. Chang K-C, et al.

Arch. Pharm. Res. 7(2) , 133-36, (1984)

Synthesis and dopamine receptor selectivity of the benzyltetrahydroisoquinoline, (R)-(+)-nor-roefractine.

J. Nat. Prod. 61(6) , 709-12, (1998)

(R)-(+)-nor-Roefractine (1) was synthesized by the Bischler-Napieralski route, using asymmetric reduction of the 1, 2-didehydro precursor imine with sodium (S)-N-CBZ-prolinyloxyborohydride. Compound 1...

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