397870-04-1

Basic information

• Product Name: Hydrazinecarboxylic acid, 2-pentyl-, 1,1-dimethylethyl ester (9CI)
• Synonyms: Hydrazinecarboxylic acid, 2-pentyl-, 1,1-dimethylethyl ester (9CI)
• CAS NO: 397870-04-1
• Molecular Formula: C₁₀H₂₂N₂O₂
• Molecular Weight: 202.29388
• Product Categories: N-BOC
• Mol File: 397870-04-1.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Hydrazinecarboxylic acid, 2-pentyl-, 1,1-dimethylethyl ester (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Hydrazinecarboxylic acid, 2-pentyl-, 1,1-dimethylethyl ester (9CI)(397870-04-1)
• EPA Substance Registry System: Hydrazinecarboxylic acid, 2-pentyl-, 1,1-dimethylethyl ester (9CI)(397870-04-1)

Safety Data

• Hazardous Substances Data: 397870-04-1(Hazardous Substances Data)

Upstream product

• 870-46-2 t-butoxycarbonylhydrazine 
• 109-52-4 valeric acid 
• 110-62-3 pentanal 
• 397870-05-2 t-butyl-2-pentylidenhydrazinecarboxylate 
• 57699-53-3 N^α-isobutyl-N^β-Boc-hydrazine 

Downstream Products

• 1372807-66-3 C₂₈H₃₉N₃O₅ 
• 1372807-99-2 (S)-4,5-dibenzyl-2-pentyl-1,2,4-triazine-3,6-dione 
• 1119-68-2 pentylhydrazine hydrochloride 

Relevant articles and documents

PHARMACEUTICAL COMPOUNDS

Compounds of formula (I): wherein: A, R, T, Q, L, Z, G, X and A′ are as defined in the description.B and D, equal to or different from each other, are selected between heteroaryl and aryl, wherein at least one of the hydrogen atoms of said heteroaryl and aryl are substituted with groups selected from SO3?, SO3H, COO?, COOH, and one or more of the other hydrogen atoms of said heteroaryl and aryl are optionally substituted as reported in the description.

Combinatorial aid for underprivileged scaffolds: Solution and solid-phase strategies for a rapid and efficient access to novel aza-diketopiperazines (aza-DKP)

An efficient solution-phase synthesis of aza-diketopiperazines (aza-DKP, triazinediones) is reported. A structurally diverse collection of c-[aza-alkylGly-Pro] derivatives and yet unreported 2,4,5-trisubstituted-1,2,4- triazine-3,6-diones has been synthesized starting from Fmoc-l-Pro-OH and various Fmoc-l-amino acids. To extend the practical value of this class of dipeptidomimetics, a general solid-phase synthesis approach amenable to library production was developed on both Wang-PS and HMBA-PS resins. The final acidic treatment of the resins in TFA/water mixture at room temperature enabled the rapid and quantitative cyclization/release highly pure triazinediones. The conformational preferences and the spatial organization of the three substituents of a representative 2,4,5-trisubstituted-1,2,4-triazine-3,6-dione were investigated by X-ray diffraction and 1H NMR spectroscopy.

Novel azapeptide inhibitors of hepatitis C virus serine protease

Azapeptides are known inhibitors of several serine and cysteine proteases. In seeking different classes of inhibitors for the HCV serine protease, a series of novel azapeptide-based inhibitors were investigated which incorporated noncleavable P1/P1′ aza-a