29791-96-6

Basic information

• Product Name: Polybenzoxazol
• Synonyms: Polybenzoxazol
• CAS NO: 29791-96-6
• Molecular Formula: MW:
• Molecular Weight: 119.12
• Mol File: 29791-96-6.mol
• Article Data: 107

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Polybenzoxazol(CAS DataBase Reference)
• NIST Chemistry Reference: Polybenzoxazol(29791-96-6)
• EPA Substance Registry System: Polybenzoxazol(29791-96-6)

Safety Data

• Hazardous Substances Data: 29791-96-6(Hazardous Substances Data)

Upstream product

• 77287-34-4 formamide 
• 95-55-6 2-amino-phenol 
• 67-56-1 methanol 
• 88-75-5 2-hydroxynitrobenzene 
• 122-51-0 orthoformic acid triethyl ester 
• 2382-96-9 benzo[d]oxazole-2-(3H)-thione 
• 13519-78-3 2-ethoxy-N-allylaniline 
• 15258-47-6 2-methoxy-N-allylaniline 
• 2369-93-9 4-phenylquinazoline 3-oxide 
• 17672-23-0 3,6-dimethyl-2-aminophenol 
• 2843-27-8 N-(2-hydroxyphenyl)formamide 
• 644-97-3 Dichlorophenylphosphine 
• 513-81-5 2,3-dimethyl-buta-1,3-diene 
• 119072-55-8 tert-butylisonitrile 

Downstream Products

• 68370-74-1 1-benzoyl-2-(2-oxo-2,3-dihydro-indol-3-yl)-2,3-dihydro-benzooxazole 
• 61933-98-0 1-phenyl-3-methyl-4-(3-acetyl-2-benzoxazolyl)-5-pyrazolone 
• 30831-96-0 2-methoxy-benzooxazole-3-carboxylic acid ethyl ester 
• 1792-52-5 (3-oxo-3,4-dihydro-benz[1,4]oxazin-2-ylidene)acetic acid methyl ester 
• 6296-59-9 2-(benzamido)phenyl benzoate 
• 222313-83-9 1-(1,3-benzoxazol-2-yl)-2,2,2-trifluoroethanone 
• 16303-58-5 5,5'-dimethyl-2,2'-dithiophene 
• 16155-56-9 2-(5-methylthiophen-2-yl)benzoxazole 
• 6797-49-5 2-butylbenzo[d]oxazole 
• 20852-38-4 N,N-diethylbenzoxazol-2-amine 
• 21326-84-1 N-butylbenzo[d]oxazol-2-amine 
• 28455-42-7 2-(isopropylamino)benzoxazole 
• 21326-91-0 2-Ethylaminobenzoxazol 
• 5998-50-5 2-(4-(tert-butyl)phenyl)benzo[d]oxazole 

Relevant articles and documents

Synthetic Applications of a New Magnetic Mesoporous Nanocomposite Catalyst Fe3O4@MCM-41@NH-SO3H

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Application of [PVP-SO3H] HSO4 as an Efficient Polymeric-Based Solid Acid Catalyst in the Synthesis of Some Benzimidazole Derivatives

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Synthesis of isocyanides by reacting primary amines with difluorocarbene

A general, convenient, and friendly route for preparing a versatile building block of isocyanides from primary amines is developed. Difluorocarbene, generated in situ from decarboxylation of chlorodifluoroacetate, reacts efficiently with primary amines to produce isocyanides. Various primary amines are well tolerated, including aryl, heteroaryl, benzyl, and alkyl amines, as well as amine residues in amino acids and peptides. Late-stage functionalization of biologically active amines is demonstrated, showing its practical capacity in drug design and peptide modification.