Detail of > 1501-26-4
- MSDS Download

- CAS Number:
- 1501-26-4
- Name:
Pentanoic acid,5-chloro-5-oxo-, methyl ester
- Superlist Name:
- Methyl 4-(chloroformyl)butyrate
- Formula:
- C6H9ClO3
- Molecular Structure:

- Synonyms:
- 4-(Chlorocarbonyl)butanoic acidmethyl ester;4-(Methoxycarbonyl)butyryl chloride;4-Chlorocarbonylbutyric acidmethyl ester;5-Chloro-5-oxopentanoic acid methyl ester;Glutaric acidmonomethyl ester chloride;Glutaryl chloride methyl ester;Methyl4-(chlorocarbonyl)butanoate;Methyl 4-(chloroformyl)butanoate;Methyl 5-chloro-5-oxopentanoate;Methyl5-chloro-5-oxovalerate;Methyl glutaroyl chloride;Methyl glutaryl chloride;NSC 93892;g-(Carbomethoxy)butyryl chloride;4-(Carbomethoxy)butanoylchloride;4-(Carbomethoxy)butyryl chloride;
- Molecular Weight:
- 164.59
- EINECS:
- 216-115-6
- Density:
- 1.179 g/cm3
- Boiling Point:
- 224 °C at 760 mmHg
- Flash Point:
- 82.2 °C
- Solubility:
- reacts with water
- Appearance:
- clear colourless to light yellow liquid
- Hazard Symbols:
C- Risk Codes:
- 34
- Safety:
- 26-36/37/39-45-24/25Details
- Transport Information:
- UN 3265 8/PG 2
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Reference
- A new general method for the synthesis of lipoxygenase products: preparation of (±)-5-HETE
- A new general method for the synthesis of lipoxygenase products: preparation of (±)-5-HETE. Rokach, Joshua; Adams, Julian; Perry, Richard (Merck Frosst Canada Inc., Pointe Claire-Dorval, PQ H9R 4P8, Can.Chemicals with cas numbers 1501-26-4 and 89682-42-8 also play role.). Tetrahedron Lett., 24(47), 5185-8 (English) 1983. CODEN: TELEAY. ISSN: 0040-4039. DOCUMENT TYPE: Journal CA Section: 26 (Biomolecules and Their Synthetic Analogs) w-Formylalkanoate esters were proposed as synthons for the title compds. In particular, com. available ClCO(CH2)3CO2Me was used to synthesize 6E,8E,11Z,14Z-(±)-5-hydroxy-6,8,11,14-eicosatetraenoic acid (I). .
- Synthesis, characterisation and properties of bismuth(III) ester pendant arm picket porphyrins
- Some chemicals with cas registry numbers like 645389-11-3 and 1501-26-4 are also used. Synthesis, characterisation and properties of bismuth(III) ester pendant arm picket porphyrins. Halime, Zakaria; Michaudet, Lydie; Razavet, Mathieu; Ruzie, Christian; Boitrel, Bernard (Institut de Chimie, UMR CNRS 6509, Campus de Beaulieu, Universite de Rennes 1, Rennes 35042, Fr.). Dalton Transactions, (22), 4250-4254 (English) 2003 Royal Society of Chemistry. CODEN: DTARAF. ISSN: 1477-9226. DOCUMENT TYPE: Journal CA Section: 78 (Inorganic Chemicals and Reactions) Section cross-reference(s): 26, 75 Porphyrins bearing a variety of ester pendant arms were synthesized. The no. of potential coordinating groups was varied from one to four. In the case of the four-picket compds., the arm length was also studied. Structural properties towards the coordination of the bismuth(III) cation were studied. In the particular case of the two-picket mols., the substitution isomers (5,10 or 5,15) were also prepd. An improvement of the rate of metalation was detected in the case of the single-picket porphyrin. .
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