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IODOETHANE-D5, also known as Labeled 1-Iodoethane, is a clear colorless liquid with unique chemical properties. It is a deuterated variant of iodoethane, which means it contains deuterium atoms instead of regular hydrogen atoms. This characteristic makes it particularly useful in various chemical applications, including organic synthesis and electrochemical reactions.

6485-58-1

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6485-58-1 Usage

Uses

Used in Organic Synthesis:
IODOETHANE-D5 is used as a reagent for the synthesis of disubstituted α-amino acids through alkylation reactions. Its deuterated nature provides specific advantages in the reaction process, such as improved reaction rates or selectivity, making it a valuable tool in organic chemistry.
Used in Electrochemical Reduction:
IODOETHANE-D5 is also utilized in electrochemical reduction reactions, specifically in the preparation of carbamates. The deuterium labeling allows for better control and understanding of the reaction mechanisms, which can be crucial in optimizing the process and improving the overall yield of the desired product.

Check Digit Verification of cas no

The CAS Registry Mumber 6485-58-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,8 and 5 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6485-58:
(6*6)+(5*4)+(4*8)+(3*5)+(2*5)+(1*8)=121
121 % 10 = 1
So 6485-58-1 is a valid CAS Registry Number.
InChI:InChI=1/C2H5I/c1-2-3/h2H2,1H3/i1D3,2D2

6485-58-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,1,2,2-pentadeuterio-2-iodoethane

1.2 Other means of identification

Product number -
Other names per-deuterated ethyl iodide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:6485-58-1 SDS

6485-58-1Upstream product

6485-58-1Relevant academic research and scientific papers

Mechanistic Investigation of Carbon-Carbon Bond Formation in the Reduction of Alkyl Halides by Organonickel Complexes in Aqueous Solution

Bakac, Andreja,Espenson, James H.

, p. 719 - 723 (2007/10/02)

The macrocyclic alkylnickel(II) complexes, RNi(tmc)+ (R = C2H5, C3H7, and CH2-c-C5H9; tmc = (1R,4R,8S,11S)-1,4,8,11-tetramethyl-1,4,8.11-tetraazacyclotetradecane), react with alkyl halides R'X (R'= CH3, C2H5, 1-C3H7, 2-C3H7, and PhCH2) in alkaline aqueous solutions, yielding combination and disproportionation products of R and R'.The reactivity of R'X increases in the order methyl . + 2-C3H7I -> 2-C3H7. + C2H5I in aqueous solution was determined by competition with V(H2O)62+.The value k2-PrI ca. 6E5 M-1s-1 is significantly higher than in aprotic solvents.

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