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534-08-7

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534-08-7 Usage

General Description

1,3-diiodopropan-2-ol is a chemical compound with the molecular formula C3H7I2O. It is commonly used as an intermediate in organic synthesis, where it acts as a building block for the creation of other compounds. This particular chemical is characterized by its three-carbon chain with a hydroxyl group and two iodine atoms attached to the second carbon atom. The presence of iodine in its structure makes 1,3-diiodopropan-2-ol a valuable reagent in organic chemistry, particularly in the synthesis of pharmaceuticals and fine chemicals. Additionally, it is also utilized in the preparation of various derivatives and is considered a versatile and important chemical in the field of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 534-08-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,3 and 4 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 534-08:
(5*5)+(4*3)+(3*4)+(2*0)+(1*8)=57
57 % 10 = 7
So 534-08-7 is a valid CAS Registry Number.
InChI:InChI=1/C3H6I2O/c4-1-3(6)2-5/h3,6H,1-2H2

534-08-7Relevant articles and documents

Expeditious Syntheses to Pharmochemicals 1,3-Dihydroxyacetone, 1,3-Dichloro-, 1,3-Dibromo- And 1,3-Diiodoacetone from Glycerol 1,3-Dichlorohydrin Using Homogenous and Heterogenous Medium

Pereira, Vera Lúcia P.,da Silva, Fernanda Priscila N. R.,da Silva, Sara R. B.,dos Santos, Priscila F.

, p. 1725 - 1731 (2020/10/09)

New efficient and reproductive routes to production of 1,3-dihydroxyacetone (1), 1,3-dichloroacetone (6), 1,3-dibromoacetone (7) and 1,3-diiodoacetone (8) from glycerol 1,3-dichlorohydrin (3) were developed. The synthesis of 1 was processed in three steps from glycerol 2 (1,3-selective chlorination of 2 to 3, oxidation of 3 to 6 and subsequent di-hydroxylation) in 51% overall yield. On the other hand, 7 and 8 were produced from 3, via a trans-bromination and trans-iodination, respectively, followed by oxidation and hydroxylation steps, in 38-52% overall yield. It was used homogeneous media with different reagents (HCl/AcOH, pyridinium chlorochromate (PCC), PCC-HIO4) and heterogeneous media with reagents supported on polymer resins such as Amberlyst A26-HCrO4– form, PV-PCC (polyvinyl-pyridinium chlorochromate) and Amberlyst A26-OH– form or reagents supported on alumina such as KI/Al2O3, KBr/Al2O3, in solvent free conditions.

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