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6485-58-1

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6485-58-1 Usage

Chemical Properties

clear colorless liquid

Uses

Different sources of media describe the Uses of 6485-58-1 differently. You can refer to the following data:
1. (Iodoethane-d5) Labeled 1-Iodoethane, which is used in a variety of organic chemical reactions including the synthesis if disubstituted α-amino acids through alkylation reaction. Also used in electrochemical reduction reactions in the preparation of carbamates.
2. Labeled 1-Iodoethane, which is used in a variety of organic chemical reactions including the synthesis if disubstituted α-amino acids through alkylation reaction. Also used in electrochemical reduction reactions in the preparation of carbamates.

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 articles and documents

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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