CAS No.32161-06-1,4-Piperidinone,1-acetyl- Suppliers,MSDS download

Detail of "32161-06-1"

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CAS Number:

32161-06-1

Name:

4-Piperidinone,1-acetyl-

Superlist Name:

N-Acetyl-4-piperidone

Molecular Structure:

Formula:

C₇H₁₁NO₂

Molecular Weight:

141.17

Synonyms:

4-Piperidone,1-acetyl- (6CI,8CI);1-Acetyl-4-oxopiperidine;1-Acetyl-4-piperidinone;1-Acetyl-4-piperidone;N-Acetyl-4-piperidinone;N-Acetyl-4-piperido;

EINECS:

250-937-6

Density:

1.126 g/cm³

Boiling Point:

218.8 °C at 760 mmHg

Flash Point:

87.9 °C

Appearance:

clear orange oily liquid

Hazard Symbols:

Risk Codes:

36/37/38

Safety:

23-24/25-36-26 Details

Reference

Reactivity in aqueous basic medium of N-acyl 4-piperidones, soluble and fixed on a polyacrylamide support: hydration and aldolization: Reactivity in aqueous basic medium of N-acyl 4-piperidones, soluble and fixed on a polyacrylamide support: hydration and aldolization. Sola, R.; Brugidou, J.; Taillades, J.; Commeyras, A. (Univ. Sci. Tech. Languedoc, Montpellier 34060, Fr.). Nouv. J. Chim., 10(8-9), 499-506 (French) 1986. CODEN: NJCHD4. ISSN: 0398-9836. DOCUMENT TYPE: Journal CA Section: 37 (Plastics Manufacture and Processing) Section cross-reference(s): 34, 35, 38 Immobilization of 1-acyl-4-piperidone hydration catalysts (for amino acid manuf. from a-aminonitriles) on acrylamide polymers, did not affect the hydration equil. of the piperidones significantly. However, the network structure of crosslinked polyacrylamides suppressed intraresin trimerization which would result in catalyst deactivation.In this experiment, several chemicals are used like 32161-06-1 and 108490-17-1 Intraresin dimerization was not inhibited by crosslinking. Crosslinking affected the intraresin aldol formation. The use of crosslinked resins improved the site isolation of the catalysts. .

Synthesis and bioactivities of novel bicyclic thiophenes and 4,5,6,7-tetrahydrothieno[2,3-c]pyridines as inhibitors of tumor necrosis factor-a (TNF-a) production: Synthesis and bioactivities of novel bicyclic thiophenes and 4,5,6,7-tetrahydrothieno[2,3-c]pyridines as inhibitors of tumor necrosis factor-a (TNF-a) production. Fujita, Masakazu; Seki, Taketsugu; Ikeda, Naoko (Pharmaceutical Research Laboratories, Nikken Chemicals Co., Saitama-shi, Saitama 330-0835, Japan). Bioorganic & Medicinal Chemistry Letters, 12(15), 1897-1900 (English) 2002 Elsevier Science Ltd. CODEN: BMCLE8. ISSN: 0960-894X.Several substances like 79-30-1 may be metioned in this study.In this article, certain chemicals are used. Some of their cas registry numbers are 487412-57-7 and 32161-06-1 DOCUMENT TYPE: Journal CA Section: 28 (Heterocyclic Compounds (More Than One Hetero Atom)) Section cross-reference(s): 1 Bicyclic thiophenes and 4,5,6,7-tetrahydrothieno[2,3-c]pyridine derivs. were synthesized and evaluated for their ability to inhibit LPS-stimulated prodn. of TNF-a. Several compds. revealed excellent in vivo activity. Furthermore, one compd. was found effective in adjuvant-induced arthritis in the rat. ..

Detail of "32161-06-1"

4-Piperidinone,1-acetyl-

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CAS No.32161-06-1 N-Acetyl-4-piperidone

CAS No.32161-06-1 N-Acetyl-4-piperidone

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CAS No.32161-06-1 N-Acetyl-4-piperidone

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CAS No.32161-06-1 N-Acetyl-4-piperidone

CAS No.32161-06-1 N-Acetyl-4-piperidone

CAS No.32161-06-1 N-Acetyl-4-piperidone

CAS No.32161-06-1 N-Acetyl-4-piperidone

CAS No.32161-06-1 N-Acetyl-4-piperidone

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CAS No.32161-06-1 N-Acetyl-4-piperidone

CAS No.32161-06-1 N-Acetyl-4-piperidone

CAS No.32161-06-1 N-Acetyl-4-piperidone

CAS No.32161-06-1 N-Acetyl-4-piperidone

CAS No.32161-06-1 N-Acetyl-4-piperidone

CAS No.32161-06-1 N-Acetyl-4-piperidone

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