Ethyl Glutaryl Chloride

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Names

[ CAS No. ]:
5205-39-0

[ Name ]:
Ethyl Glutaryl Chloride

[Synonym ]:
Glutaric Acid Monoethyl Ester Chloride
Ethyl 4-(Chloroformyl)butyrate
MFCD00013659
Ethyl 5-chloro-5-oxopentanoate
Ethyl glutaryl chloride
EINECS 226-000-2

Chemical & Physical Properties

[ Density]:
1.144g/cm3

[ Boiling Point ]:
230ºC at 760mmHg

[ Molecular Formula ]:
C7H11ClO3

[ Molecular Weight ]:
178.61300

[ Flash Point ]:
92.6ºC

[ Exact Mass ]:
178.04000

[ PSA ]:
43.37000

[ LogP ]:
1.48520

[ Appearance of Characters ]:
Liquid

[ Index of Refraction ]:
n20/D 1.443

[ Storage condition ]:
2-8°C

[ Water Solubility ]:
Soluble in water.

MSDS

Safety Information

[ Symbol ]:

GHS05

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H314

[ 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

[ Risk Phrases ]:
34-37

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

[ RIDADR ]:
UN 3265 8/PG 2

[ WGK Germany ]:
3

[ Packaging Group ]:
III

[ HS Code ]:
2918300090

Synthetic Route

Customs

[ HS Code ]: 2918300090

[ Summary ]:
2918300090 other carboxylic acids with aldehyde or ketone function but without other oxygen function, their anhydrides, halides, peroxides, peroxyacids and their derivatives。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:6.5%。General tariff:30.0%

Articles

Synthesis and evaluation of some lipidic aminoalcohols and diamines as immunomodulators.

Bioorg. Med. Chem. Lett. 16(23) , 6091-5, (2006)

Lymphoproliferation inhibition and cytotoxicity of a number of lipidic aminoacids, aminoalcohols and diamines were evaluated as a preliminary screening to select potential immunomodulators. The four m...

Synthesis of Several Diester Group-Containing Calix [4] arenes. Nam KC, et al.

Bull. Korean Chem. Soc. 17(6) , 502-506, (1996)


More Articles


Related Compounds

  • METHYL GLUTARYL CHLORIDE
  • 3-methyl glutaryl chloride
  • Chloroethane-13C2
  • 2-(trimethylsilyl)ethyl chloride
  • 2-(p-benzyloxyphenyl)-ethyl chloride
  • 1-(4-methylphenyl)ethyl chloride
  • Tert-butyl 4-(4-(4-chloro-1,3,5-triazin-2-ylamino)phenyl)piperidine-1-carboxylate
  • (4-Amino-2-methoxyphenyl)(4-(oxetan-3-yl)piperazin-1-yl)methanone
  • 4-(5-Methoxy-2-piperidinyl)benzonitrile
  • 4-chloro-N-(3-morpholinophenyl)-1,3,5-triazin-2-amine
  • 4-Chloro-N-[4-[4-(tetrahydro-2h-pyran-4-yl)-1-piperazinyl]phenyl]-1,3,5-triazin-2-amine
  • 7-Pyrrolo[2,3-c]pyridin-1-yl-1,2,3,4-tetrahydro-1,6-naphthyridine
  • 4-chloro-N-(3-methoxy-4-(4-morpholinopiperidin-1-yl)phenyl)-1,3,5-triazin-2-amine
  • Methyl 4-((2R,4R)-4-methoxypiperidin-2-yl)benzoate
  • 2-(4-Fluorophenyl)-4-oxo-1-piperidinecarboxylic acid phenyl ester
  • 5-(4-((2-oxo-2,3-dihydrobenzo[d]oxazol-5-yl)amino)-1,3,5-triazin-2-yl)-2-((tetrahydro-2H-pyran-4-yl)oxy)benzonitrile
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