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261610-100ML
CYANOGEN BROMIDE 5.0M SOLUTION IN ACETONITRILE
Price: $216.26List Price: $240.29Cyanogen bromide solution induces template-guided condensation of oligonucleotides only in the presence of N -substituted morpholines . Mechanism of the phosphomonoester group activation by cyanogen bromide in N -substituted morpholine buffers has -
C725901-100mg
CYCLOBUTANE-1,1-DICARBOXYLIC ACID MONOAMIDE (C09-1584-024)
Price: $27.80List Price: $30.89CYCLOBUTANE-1,1-DICARBOXYLIC ACID MONOAMIDE. -
C725901-1g
CYCLOBUTANE-1,1-DICARBOXYLIC ACID MONOAMIDE (C09-1584-025)
Price: $97.80List Price: $108.67CYCLOBUTANE-1,1-DICARBOXYLIC ACID MONOAMIDE. -
C725901-250mg
CYCLOBUTANE-1,1-DICARBOXYLIC ACID MONOAMIDE (C09-1584-026)
Price: $39.80List Price: $44.22CYCLOBUTANE-1,1-DICARBOXYLIC ACID MONOAMIDE. -
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C167443-1g
CYCLOBUTANECARBOXAMIDE (C09-0805-704)
Price: $210.36List Price: $233.73CYCLOBUTANECARBOXAMIDE. -
C167443-250mg
CYCLOBUTANECARBOXAMIDE (C09-0805-705)
Price: $117.52List Price: $130.58CYCLOBUTANECARBOXAMIDE. -
C167443-5g
Cyclobutanecarboxamide (C09-1940-208)
Price: $430.28List Price: $478.09Cyclobutanecarboxamide -
C96001-1G
CYCLOBUTANONE 99% (C15-1207-307)
Price: $97.63List Price: $108.48Application Starting material for a new, efficient synthesis of aminocyclobutanecarboxylic acid via the intermediacy of sulfonyloxiranes. -
C96001-5G
CYCLOBUTANONE 99% (C15-1207-308)
Price: $300.36List Price: $333.74Application Starting material for a new, efficient synthesis of aminocyclobutanecarboxylic acid via the intermediacy of sulfonyloxiranes. -
161470-50G
CYCLOHEXANEPROPIONIC ACID 99%
Price: $693.24List Price: $770.27Application 3-Cyclohexanepropionic acid can be used: As a starting material in the synthesis of 2-[(1,2,4-triazol-3-yl)thio]acetamide derivatives for in vitro paraoxonase-1 (PON1) studies. To synthesize chemical intermediates such as -
133302-1G
CYCLOHEXYL ISOCYANIDE 98% (C15-1293-182)
Price: $136.60List Price: $151.78Cyclohexyl isocyanide reacts with dimethyl acetylenedicarboxylate to give a mixture of cyclopenta[ b ]pyridine derivatives, azaspirononatriene derivative and the azabicyclononatriene . It reacts with dialkyl acetylenedicarboxylates to form 1:1