(1S,2S)-trans-N-Boc-2-aminocyclopentanol

• Catalog No.: 671436
• CAS Number: 145106-43-0
• M. F.: C10H19NO3
• M. W.: 201.26276
• Purity: ≥98.5% (GC)

SYNONYMS

• Title: (1S,2S)-反式-N-Boc-2-氨基环戊醇
• IUPAC name: tert-butyl N-[(1S,2S)-2-hydroxycyclopentyl]carbamate
• IUPAC Traditional name: tert-butyl N-[(1S,2S)-2-hydroxycyclopentyl]carbamate
• Synonyms: ((1S,2S)-2-Hydroxycyclopentyl)carbamic acid tert-butyl ester; tert-Butyl N-((2S,1S)-2-hydroxycyclopentyl)carbamate

DATABASE IDS

• CAS Number: 145106-43-0
• Beilstein Number: 5810036
• MDL Number: MFCD11656038

PROPERTIES

• Empirical Formula (Hill Notation): C10H19NO3
• Optical Purity: enantiomeric ratio: ≥95:5%
• Purity: ≥98.5% (GC)
• Purity: 99%
• GHS Signal Word: Warning
• GHS Hazard statements: H302-H400
• European Hazard Symbols: Harmful (Xn)
• European Hazard Symbols: Nature polluting (N)
• Personal Protective Equipment: dust mask type N95 (US), Eyeshields, Gloves
• GHS Precautionary statements: P273
• RID/ADR: UN 3077 9/PG 3
• Risk Statements: 22-50
• Safety Statements: 61
• Storage Temperature: 2-8°C
• Hazard Class: 9
• UN Number: 3077
• Packing Group: 3
• German water hazard class: 3

DETAILS

Description (English)

Packaging
1 g in glass bottle
250 mg in glass bottle
Application
Reactant for:
• Asymmetric synthesis of constrained (-)-S-adenosyl-L-homocysteine (SAH) analogs as DNA methyltransferase inhibitors via stereoselective thioesterification, thioetherification, hydrolysis, heterocyclization and amination1

Description (简体中文)

包装
1 g in glass bottle
250 mg in glass bottle
Application
Reactant for:
• Asymmetric synthesis of constrained (-)-S-adenosyl-L-homocysteine (SAH) analogs as DNA methyltransferase inhibitors via stereoselective thioesterification, thioetherification, hydrolysis, heterocyclization and amination1