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1-(benzenesulfonyl)ethylsulfonylbenzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 33419-26-0 Structure
  • Basic information

    1. Product Name: 1-(benzenesulfonyl)ethylsulfonylbenzene
    2. Synonyms:
    3. CAS NO:33419-26-0
    4. Molecular Formula: C14H14O4S2
    5. Molecular Weight: 310.395
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 33419-26-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 548.7°Cat760mmHg
    3. Flash Point: 364.9°C
    4. Appearance: N/A
    5. Density: 1.324g/cm3
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1-(benzenesulfonyl)ethylsulfonylbenzene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(benzenesulfonyl)ethylsulfonylbenzene(33419-26-0)
    11. EPA Substance Registry System: 1-(benzenesulfonyl)ethylsulfonylbenzene(33419-26-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 33419-26-0(Hazardous Substances Data)

33419-26-0 Usage

Chemical family

Organic sulfones

Physical state

White to off-white powder

Melting point

140-143°C

Applications

a. Building block in organic synthesis
b. Production of pharmaceuticals
c. Production of agrochemicals
d. Production of specialty chemicals
e. Plastics and polymers industry
f. Synthesis of novel materials
g. Medicinal chemistry and drug discovery

Safety precautions

Handle with care due to potential hazards if not properly managed

Check Digit Verification of cas no

The CAS Registry Mumber 33419-26-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,4,1 and 9 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 33419-26:
(7*3)+(6*3)+(5*4)+(4*1)+(3*9)+(2*2)+(1*6)=100
100 % 10 = 0
So 33419-26-0 is a valid CAS Registry Number.

33419-26-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1-Bis-benzolsulfonyl-aethan

1.2 Other means of identification

Product number -
Other names Aethyliden-bis-phenylsulfon

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:33419-26-0 SDS

33419-26-0Relevant articles and documents

Dynamic Control of Chiral Space Through Local Symmetry Breaking in a Rotaxane Organocatalyst

Dommaschk, Marcel,Echavarren, Javier,Leigh, David A.,Marcos, Vanesa,Singleton, Thomas A.

supporting information, p. 14955 - 14958 (2019/11/05)

We report on a switchable rotaxane molecular shuttle that features a pseudo-meso 2,5-disubstituted pyrrolidine catalytic unit on the axle whose local symmetry is broken according to the position of a threaded benzylic amide macrocycle. The macrocycle can

Bis(phenylsulfonyl)methane mediated synthesis of olefins: Via a halogen elimination and double bond migration

Hu, Yanwei,Jiang, Jing,Hu, Ying,Cai, Xin,Wang, Liudi,Chen, Shaohua,Zhang, Shilei,Zhang, Yinan

, p. 2619 - 2622 (2018/04/27)

An effective dehydrochlorination of bis(phenylsulfonyl)alkane to prepare alkene building blocks is developed. The elimination together with double bond migration results in a variety of β,γ-unsaturated bis(phenylsulfonyl)olefins in good yields with only E geometry. The following chemical diversification represents an easy and straightforward access to a series of alkene building blocks.

Synthesis with sulfones, Part XLIII. Preparation of γ-functionalized vinyl sulfones by nucleophilic substitution of allylidene disulfones; stereospecific reduction of 3-hydroxy-(E)-1-propenyl sulfones to (Z)-allylic alcohols

Cuvigny, T.,Penhoat, C. Herve du,Julia, M.

, p. 409 - 421 (2007/10/02)

The substitution of a sulfonyl moiety ao allylidene disulfones by various nucleophiles (PhSNa, PhSO2Na, H2O and R2NH) leads to γ-functionalized (E)-vinyl sulfones.The stereospecific reduction of 3-hydroxy-(E)-1-propenyl sulfones affords (Z)-allylic alcoho

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