101625-10-9

Basic information

• Product Name: BENZYL (4-BROMOBUTYL)CARBAMATE
• Synonyms: BENZYL (4-BROMOBUTYL)CARBAMATE;Benzyl N-(4-bromobutyl)carbamate
• CAS NO: 101625-10-9
• Molecular Formula: C₁₂H₁₆BrNO₂
• Molecular Weight: 286.18
• Mol File: 101625-10-9.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 398.8±35.0 °C(Predicted)
• Appearance: /
• Density: 1.338±0.06 g/cm3(Predicted)
• PKA: 12.55±0.46(Predicted)
• CAS DataBase Reference: BENZYL (4-BROMOBUTYL)CARBAMATE(CAS DataBase Reference)
• NIST Chemistry Reference: BENZYL (4-BROMOBUTYL)CARBAMATE(101625-10-9)
• EPA Substance Registry System: BENZYL (4-BROMOBUTYL)CARBAMATE(101625-10-9)

Safety Data

• Hazardous Substances Data: 101625-10-9(Hazardous Substances Data)

Upstream product

• 501-53-1 benzyl chloroformate 
• 558-13-4 carbon tetrabromide 
• 17996-13-3 benzyl 4-hydroxybutylcarbamate 
• 128-08-5 N-Bromosuccinimide 
• 24566-81-2 4-bromo-n-butan-1-amine hydrobromide 

Downstream Products

• 688790-65-0 all-cis-3,5-N,N-di-tert-butyloxycarbonyl-1-N-[4-N-(benzyloxycarbonyl)aminobutyl]-1,3,5-triaminocyclohexane 
• 25070-74-0 1-benzyloxycarbonylpyrrolidine 
• 330934-37-7 diethyl 2-(4-benzyloxycarbonylaminobutyl)malonate 
• 167170-23-2 2-Ethoxycarbonylmethyl-piperidine-1-carboxylic acid benzyl ester 

Relevant articles and documents

Toward Efficient Zn(II)-Based Artificial Nucleases

A series of cis-cis-triaminocyclohexane Zn(II) complex-anthraquinone intercalator conjugates, designed in such a way to allow their easy synthesis and modification, have been investigated as hydrolytic cleaving agents for plasmid DNA. The ligand structure

Selective synthesis and kinetic measurement of 1:1 and 2:2 cyclic compounds containing 1,4,7,10-tetraazacyclododecane and azobenzene units

1:1 cyclic compounds 8a-c (51-55%) and 2:2 cyclic compounds 9a-c (20-49%) containing 1,4,7,-10-tetraazacyclododecane (cyclen) and azobenzene units were selectively synthesized under UV irradiation (330 nm ?, ΔH?, and ΔS?) of 8a-c and 9a-c were studied in nonpolar media (benzene) and polar media (methanol). The cis to trans isomerization rates in the dark for these cyclic compounds increase with ring size or structural flexibility (8a ? dominates ΔG? in cyclic compounds.

SUBSTITUTED PROLINE COMPOUNDS, COMPOSITION AND METHOD OF USE

Compounds of the formula STR1 are disclosed. These compounds are useful as hypotensive agents due to their angiotensin converting enzyme inhibition activity and depending upon the definition of X may also be useful as analgesics due to their enkephalinase inhibition activity.