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CDS021744-25MGOther Notes Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of unique chemicals. Sigma-Aldrich does not collect analytical data for this product.
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K3255-25MG
Sigma-Aldrich
N-(beta-Ketocaproyl)-DL-homoserine lactone (C15-1280-468)
Price: $211.50List Price: $235.00Application N -(β-Ketocaproyl)-DL-homoserine lactone has been used as a reference standard in identifying the quorum sensing signal molecules released by the in wood samples affected by Brenneria salicis bacteria bacteria, using ultra-high -
K3255-50MG
Sigma-Aldrich
N-(beta-Ketocaproyl)-DL-homoserine lactone (C15-1280-469)
Price: $330.61List Price: $367.35Application N -(β-Ketocaproyl)-DL-homoserine lactone has been used as a reference standard in identifying the quorum sensing signal molecules released by the in wood samples affected by Brenneria salicis bacteria bacteria, using ultra-high -
83845-5G-FN-(Cyanomethyl)acetamide
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N731938-5gN-(Cyclopropylmethyl)cyclopropanamine.
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43116-5GN -(Diphenylmethyl)methylamine is a sterically hindered secondary amine. It participates in the synthesis of cyclooctene oxide.
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420697-100G
Sigma-Aldrich
N-(Methoxymethyl)-N-(trimethylsilylmethyl)benzylamine (C15-1293-150)
Price: $661.20List Price: $734.67Application Forms azomethine ylides which readily undergo [3+2] cycloaddition to α,ß-unsaturated esters affording N -benzyl substituted pyrrolidines in good yields. Reacted in asymmetric 1,3-dipolar cycloadditions in the practical, -
420697-25G
Sigma-Aldrich
N-(Methoxymethyl)-N-(trimethylsilylmethyl)benzylamine (C15-1293-151)
Price: $276.86List Price: $307.62Application Forms azomethine ylides which readily undergo [3+2] cycloaddition to α,ß-unsaturated esters affording N -benzyl substituted pyrrolidines in good yields. Reacted in asymmetric 1,3-dipolar cycloadditions in the practical, -
420697-5G
Sigma-Aldrich
N-(Methoxymethyl)-N-(trimethylsilylmethyl)benzylamine (C15-1293-152)
Price: $92.38List Price: $102.65Application Forms azomethine ylides which readily undergo [3+2] cycloaddition to α,ß-unsaturated esters affording N -benzyl substituted pyrrolidines in good yields. Reacted in asymmetric 1,3-dipolar cycloadditions in the practical, -
CBR00180-1GOther Notes Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of unique chemicals. Sigma-Aldrich does not collect analytical data for this product.
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N463314-10mgDescription:N-(p-Coumaroyl)-L-homoserine lactone, or pC-HSL, can be used to study microbiology, quorum sensing and signaling compounds. pC-HSL has been used to study the activity of the Rhodopseudomonas palustris p-coumaroyl-homoserine
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731161-1GApplication Reactant for: Preparation of allenamides by alkylation with propargyl bromide and isomerization Ugi 3CC reaction