68373-12-6

Basic information

• Product Name: BENZYL 2-IODOETHYLCARBAMATE
• Synonyms: BENZYL 2-IODOETHYLCARBAMATE
• CAS NO: 68373-12-6
• Molecular Formula: C₁₀H₁₂INO₂
• Molecular Weight: 305.11
• Mol File: 68373-12-6.mol
• Article Data: 7

Chemical Properties

• Appearance: /
• CAS DataBase Reference: BENZYL 2-IODOETHYLCARBAMATE(CAS DataBase Reference)
• NIST Chemistry Reference: BENZYL 2-IODOETHYLCARBAMATE(68373-12-6)
• EPA Substance Registry System: BENZYL 2-IODOETHYLCARBAMATE(68373-12-6)

Safety Data

• Hazardous Substances Data: 68373-12-6(Hazardous Substances Data)

Usage

General Description

Benzyl 2-Iodoethylcarbamate is a chemical compound that falls under the category of carbamate esters. It is primarily used in the field of organic synthesis. Its molecular formula is C10H12INO2 and it is typically available as a clear liquid or solid compound. Its chemical structure consists of a carbamate group bound to an iodoethyl side chain and a benzyl group. Like many other organic compounds, it must be handled with caution due to its potential reactivity and toxicity.

Upstream product

• 52689-15-3 2-iodoethylamine 
• 501-53-1 benzyl chloroformate 
• 1138-80-3 N-(Benzyloxycarbonyl)glycine 
• 55378-79-5 C₁₃H₁₅NO₆ 
• 77987-49-6 benzyl 2-hydroxyethylcarbamate 
• 53844-02-3 benzyl N-(2-bromoethyl)carbamate 

Downstream Products

• 41889-04-7 S-(2-benzyloxycarbonylamino-ethyl)-L-cysteine 
• 198756-71-7 [2-(4-Phenyl-piperazin-1-yl)-ethyl]-carbamic acid benzyl ester 
• 195314-68-2 N-benzyloxycarbonyl-2-(4-benzylpiperazin-1-yl)ethylamine 
• 189454-56-6 4-O-(3-amino-N-ethylaminobenzyloxycarbonyl-2,3-dideoxy-4,6-O-ethylidene-β-D-ribo-hexopyranosyl)-epipodophyllotoxin 
• 1252806-12-4 C₂₄H₂₇N₅O₆ 
• 146552-66-1 benzyl (2-azidoethyl)carbamate 
• 1489121-06-3 C₁₃H₁₄N₄O₄ 
• 30853-30-6 Cbz-Gly-ψ[CH₂NCS] 
• 2014-75-7 2-(phenylthio)ethanamine 
• 1458631-98-5 C₄₄H₅₀N₄O₁₀ 
• 1458631-99-6 C₇₁H₉₃N₇O₁₃ 

Relevant articles and documents

Staudinger/aza-Wittig reaction to access Nβ-protected amino alkyl isothiocyanates

A unified approach to access Nβ-protected amino alkyl isothiocyanates using Nβ-protected amino alkyl azides through a general strategy of Staudinger/aza-Wittig reaction is described. The type of protocol used to access isothiocyanates depends on the availability of precursors and also, especially in the amino acid chemistry, on the behavior of other labile groups towards the reagents used in the protocols; fortunately, we were not concerned about both these factors as precursor-azides were prepared easily by standard protocols, and the present protocol can pave the way for accessing title compounds without affecting Boc, Cbz and Fmoc protecting groups, and benzyl and tertiary butyl groups in the side chains. The present strategy eliminates the need for the use of amines to obtain title compounds and thus, this method is step-economical; additional advantages include retention of chirality, convenient handling and easy purification. A few hitherto unreported compounds were also prepared, and all final compounds were completely characterized by IR, mass, optical rotation, and 1H and 13C NMR studies.

Synthesis of Nα-Z protected amino alkyl triazole acids and their application to neo-glycopeptides synthesis

The synthesis of triazole linked glycopeptides employing 2-chloro-4,6-dimethoxy-1,3,5-triazine (CDMT) mediated coupling of Z-protected triazole acids with glycosyl amines and amino acid esters is described. The coupling proceeded smoothly at room temperat

Synthesis of Hybrid Peptidomimetics and Neoglycoconjugates Employing Click Protocol: Dual utility of Poc-group for inserting carbamate-triazole units into peptide backbone

Synthesis of new types of peptidomimetics and glycosylated amino acids possessing 1,2,3-triazole and carbamate moieties is described. Poc-protected amino acid esters/1-amino sugars were subjected to Cu(I) catalyzed [2+3]cycloaddition with desired azides u