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2-[(E)-2-Butenyl]thiophene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 52008-15-8 Structure
  • Basic information

    1. Product Name: 2-[(E)-2-Butenyl]thiophene
    2. Synonyms: 2-[(E)-2-Butenyl]thiophene
    3. CAS NO:52008-15-8
    4. Molecular Formula: C8H10S
    5. Molecular Weight: 138.23
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 52008-15-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 183.1±9.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 0.999±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-[(E)-2-Butenyl]thiophene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-[(E)-2-Butenyl]thiophene(52008-15-8)
    11. EPA Substance Registry System: 2-[(E)-2-Butenyl]thiophene(52008-15-8)
  • 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: 52008-15-8(Hazardous Substances Data)

52008-15-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52008-15-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,0,0 and 8 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 52008-15:
(7*5)+(6*2)+(5*0)+(4*0)+(3*8)+(2*1)+(1*5)=78
78 % 10 = 8
So 52008-15-8 is a valid CAS Registry Number.

52008-15-8SDS

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 2-but-2-enylthiophene

1.2 Other means of identification

Product number -
Other names 2-[(E)-2-Butenyl]thiophene

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:52008-15-8 SDS

52008-15-8Downstream Products

52008-15-8Relevant articles and documents

CU(I)-Catalyzed regioselective synthesis of substituted allyl furans and thiophenes using organostannanes

Nudelman, Norma S.,Carro, Cecilia

, p. 1942 - 1944 (2007/10/03)

2-Allyl-substituted furans and thiophenes were efficiently synthesized from organostannyl derivatives as starting materials using Cu(I) as catalyst. The effect of DMF and NMP as solvents are discussed, as well as other solvent and temperature effects.

Process for producing acylaromatic compounds

-

, (2008/06/13)

Acylaromatic compounds STR1 (Q: aromatic compound residue; R: straight, branched or cyclic aliphatic group, aromatic group or araliphatic group) are prepared in high yield by a reaction, in the presence of a boron trifluoride complex catalyst, of an aromatic compound with STR2 (X: H, Cl, Br; Y: Cl, Br) or with RCOOH in the presence of (XYCHCO)2 O.

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