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(+)-TRANS-4,5-BIS(IODOMETHYL)-2,2-DIMETHYL-1,3-DIOXOLANE is a chiral chemical compound characterized by a dioxolane ring with two iodomethyl groups attached at the 4 and 5 positions. It features a trans configuration and is known for its unique structure and reactivity, making it a valuable tool in organic chemistry research.
Used in Organic Synthesis:
(+)-TRANS-4,5-BIS(IODOMETHYL)-2,2-DIMETHYL-1,3-DIOXOLANE is used as a reagent in organic synthesis for its ability to facilitate the formation of complex molecular structures.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (+)-TRANS-4,5-BIS(IODOMETHYL)-2,2-DIMETHYL-1,3-DIOXOLANE serves as a precursor for the development of other organic compounds, potentially leading to new pharmaceutical agents.
Used in Construction of Complex Molecular Structures:
This chemical compound is utilized as a building block for constructing intricate molecular structures, which can be beneficial in various chemical and pharmaceutical applications.
It is crucial to handle (+)-TRANS-4,5-BIS(IODOMETHYL)-2,2-DIMETHYL-1,3-DIOXOLANE with care due to its potentially hazardous nature and the risk of adverse health effects if not properly managed.

58342-57-7

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58342-57-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58342-57-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,3,4 and 2 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 58342-57:
(7*5)+(6*8)+(5*3)+(4*4)+(3*2)+(2*5)+(1*7)=137
137 % 10 = 7
So 58342-57-7 is a valid CAS Registry Number.

58342-57-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (+)-TRANS-4 5-BIS(IODOMETHYL)-2,2-DIMETHYL-1 3-DIOXOLANE

1.2 Other means of identification

Product number -
Other names 1,4-Dideoxy-1,4-diiodo-2,3-O-isopropylidene-L-threitol

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:58342-57-7 SDS

58342-57-7Relevant academic research and scientific papers

NEUROLOGICALLY-ACTIVE COMPOUNDS

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Page/Page column 11; 16, (2008/06/13)

The invention provides a compound of the formula (I): wherein R is methyl, ethyl, propyl, isopropyl, butyl, pentyl, neo-pentyl or cyclohexyl, or a salt or solvate thereof. These compounds are selective GABAC receptor antagonists. The invention also provides pharmaceutical compositions comprising a compound of formula (I) or a pharmaceutically acceptable salt or solvate thereof. The invention also provides methods of enhancing the cognitive activity of an animal and methods of stimulating memory capacity in an animal, comprising the step of administering to the animal an effective amount of a compound of formula (I) or a pharmaceutically acceptable salt or solvate thereof.

An Efficient Synthesis of 4(S)-Hydroxycyclopent-2-enone

Khanapure, Subhash P.,Najafi, Nahid,Manna, Sukumar,Yang, Jing-Jing,Rokach, Joshua

, p. 7548 - 7551 (2007/10/03)

An efficient synthesis of 4(S)-hydroxycyclopent-2-enone of high optical purity, a key synthon used in natural product synthesis, is described.The method is suitable for large-scale synthesis.

Novel Copper Complexes of Chiral Diphosphines: Preparation, Structure, and Use To Form Rhodium Complex Catalysts for Chiral Hydrogenations

Townsend, John M.,Blount, John F.,Sun, Ruen Chu,Zawoiski, Sonja,Valentine, Donald

, p. 2995 - 2999 (2007/10/02)

Treatment of chiral diphosphines 5a-c and 13 ("DIOP", aryl derivatives and related substances) with CuCl in boiling ethanol gave complexes having the composition n, 6a-c and 11.Crystallizations of 6a-c from crude 70-80percent pure 5a-c and decomposition of the complexes by ammonia gave the pure diphosphines.Ligand exchange between 6a-c and 2 in methanol at 23 deg C was rapid and complete.Treatment of the resulting solutions with H2 gave active catalysts for asymmetric hydrogenations.

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