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1,4-Dibromo-2,3-butanediol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 19953-61-8 Structure
  • Basic information

    1. Product Name: 1,4-Dibromo-2,3-butanediol
    2. Synonyms: 1,4-Dibromo-2,3-butanediol;
    3. CAS NO:19953-61-8
    4. Molecular Formula: C4H8Br2O2
    5. Molecular Weight: 247.91
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 19953-61-8.mol
  • Chemical Properties

    1. Melting Point: 82-84℃
    2. Boiling Point: 365.3 °C at 760 mmHg
    3. Flash Point: 174.7 °C
    4. Appearance: /
    5. Density: 2.124 g/cm3
    6. Vapor Pressure: 8.09E-07mmHg at 25°C
    7. Refractive Index: 1.583
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 1,4-Dibromo-2,3-butanediol(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1,4-Dibromo-2,3-butanediol(19953-61-8)
    12. EPA Substance Registry System: 1,4-Dibromo-2,3-butanediol(19953-61-8)
  • Safety Data

    1. Hazard Codes:  Xi:Irritant;
    2. Statements: R37/38:; R41:;
    3. Safety Statements: S26:; S39:;
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 19953-61-8(Hazardous Substances Data)

19953-61-8 Usage

Appearance

Colorless solid

Odor

Slightly sweet

Usage

Building block in the production of other chemicals and pharmaceuticals

Role

Intermediate in the synthesis of various compounds

Industries

Pharmaceuticals, food additives, cosmetics

Safety precautions

Handle with care, harmful if ingested or inhaled, may cause skin and eye irritation

Check Digit Verification of cas no

The CAS Registry Mumber 19953-61-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,9,5 and 3 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 19953-61:
(7*1)+(6*9)+(5*9)+(4*5)+(3*3)+(2*6)+(1*1)=148
148 % 10 = 8
So 19953-61-8 is a valid CAS Registry Number.
InChI:InChI=1/C4H8Br2O2/c5-1-3(7)4(8)2-6/h3-4,7-8H,1-2H2

19953-61-8Downstream Products

19953-61-8Relevant articles and documents

Hexamethonium bis(tribromide) (HMBTB) a recyclable and high bromine containing reagent

Paul, Bappi,Bhuyan, Bishal,Purkayastha, Debraj D.,Dhar, Siddhartha S.,Patel, Bhisma K.

, p. 5646 - 5650 (2015/09/21)

A recyclable and high bromine containing di-(tribromide) reagent, hexamethonium bis(tribromide) (HMBTB) has been synthesized and utilized for the bromination of various organic substrates. The spent reagent hexamethonium bromide (HMB) can be effectively recycled by regenerating and reusing it without significant loss of activity. The crystalline and stable bis(tribromide) is an effective storehouse of very high percentage of active bromine requiring just half an equivalent of it for complete bromination. Both the Br3- moieties in HMBTB are nearly linear with Br-Br-Br angle of 179.55°.

A new recyclable ditribromide reagent for efficient bromination under solvent free condition

Kavala, Veerababurao,Naik, Sarala,Patel, Bhisma K.

, p. 4267 - 4271 (2007/10/03)

1,2-Dipyridiniumditribromide-ethane (DPTBE) has been synthesized and explored as a new efficient brominating agent. The crystalline ditribromide reagent is stable for months and acts as a safe source of bromine requiring just 0.5 equiv for complete bromination. It has high active bromine content per molecule and shows a remarkable reactivity compared to other tribromide reagents toward various substrates by just grinding the reagent and substrates in a porcelain mortar at room temperature. No organic solvent has been used during any stage of the reaction for substrates giving product as solid. Product can easily be isolated by just washing the highly water soluble 1,2- dipyridiniumdibromide-ethane (DPDBE) from the brominated product. The spent reagent can be recovered, regenerated, and reused without any significant loss.

A convenient halogenation of α,β-unsaturated carbonyl compounds with OXONE and hydrohalic acid (HBr,HCl)

Kim, Kyoung-Mahn,Park, In-Hwan

, p. 2641 - 2644 (2007/10/03)

Mixtures of OXONE and hydrobromic acid or hydrochloric acid afford solutions of bromine or chlorine, respectively, α-Bromo- or α-chloro-α,β-unsaturated carbonyl compounds were prepared by addition of hydrobromic acid or hydrochloric acid to the mixture of

Raman, infrared, and microwave spectra and conformational preferences of meso-Bisoxirane

Kalasinsky,Subramaniam,Su,Cook

, p. 521 - 530 (2007/10/03)

Vibrational infrared and Raman spectra of liquid and solid meso-bisoxirane and infrared spectra of the gaseous phase were recorded. Additionally, microwave rotational spectra from 40 to 18 GHz were recorded. The vibrational spectra demonstrate the presence of two conformations in the fluid phases but only one in the solid state. Infrared and Raman activities and gas-phase band contours indicate that the trans conformer with C(i) molecular symmetry is more stable than the gauche conformer (C1 symmetry). Variable temperature studies of two pairs of Raman lines are consistent with a ΔH value of 0.31 ± 0.10 kcal/mol in the liquid state. Rotational constants (A = 9187.45 ± 0.04, B = 2651.80 ± 0.01, C = 2608.92 ± 0.01 MHz) and the dipole moment (μ(total) = 3.03 D) were determined for the gauche conformer. Model calculations give an acceptable match to the observed rotational constants for an H-C-C'-H' dihedral angle of 60°. The relationship of meso-bisoxirane to other similar three-membered ring compounds is discussed. Published by Elsevier Science B.V.

Nickel mdiated Double Bond formation from vic-Dibromides and Ethyl Magnesium Bromide

Malanga, Corrado,Aronica, Laura A.,Lardicci, Luciano

, p. 9189 - 9192 (2007/10/02)

vic-dibromides are quantitaively converted into alkenes by using a catalityc amount of NidppeCl2 in the presence of two molar equivalents of EtMgBr in THF.Stereochemical aspects of the reaction are given.

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