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1576-85-8

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1576-85-8 Usage

Chemical Properties

Different sources of media describe the Chemical Properties of 1576-85-8 differently. You can refer to the following data:
1. clear yellow liquid
2. 4-Pentenyl acetate has a fruity aroma.

Definition

ChEBI: An acetate ester of pent-4-en-1-ol.

Check Digit Verification of cas no

The CAS Registry Mumber 1576-85-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,7 and 6 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1576-85:
(6*1)+(5*5)+(4*7)+(3*6)+(2*8)+(1*5)=98
98 % 10 = 8
So 1576-85-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H12O2/c1-3-4-5-6-9-7(2)8/h3H,1,4-6H2,2H3

1576-85-8 Well-known Company Product Price

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  • (Code)Product description
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  • Alfa Aesar

  • (B20258)  4-Penten-1-yl acetate, 98%   

  • 1576-85-8

  • 5g

  • 849.0CNY

  • Detail
  • Alfa Aesar

  • (B20258)  4-Penten-1-yl acetate, 98%   

  • 1576-85-8

  • 25g

  • 3380.0CNY

  • Detail

1576-85-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-penten-1-yl acetate

1.2 Other means of identification

Product number -
Other names 4-Pentenyl Acetate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Food additives -> Flavoring Agents
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:1576-85-8 SDS

1576-85-8Relevant articles and documents

Synthesis of the ABC Substructure of Brevenal by Sequential exo-Mode Oxacyclizations of Acyclic Polyene Precursors

Hurtak, Jessica A.,McDonald, Frank E.

, p. 6036 - 6039 (2017)

Exploratory studies on the sequential exo-mode oxacyclizations of acyclic polyene precursors have provided a substantial substructure of brevenal, including the fused tricyclic polyether with stereochemical patterns consistent with the AB and BC ring fusions. The synthesis of acyclic substrates featured two variations of Cr(II)/Ni(II) couplings for preparing 1,1-disubstituted allylic alcohols. A sequence of iodine-promoted cycloetherification, base-promoted intramolecular conjugate addition, and mercury-promoted cycloetherification produced the tricyclic substructure.

A Pd-Catalyzed [4 + 2] Annulation Approach to Fluorinated N-Heterocycles

García-Vázquez, Víctor,Hoteite, Larry,Lakeland, Christopher P.,Watson, David W.,Harrity, Joseph P. A.

supporting information, p. 2811 - 2815 (2021/05/05)

3-Fluoro- and trifluoromethylthio-piperidines represent important building blocks for discovery chemistry. We report a simple and efficient method to access analogs of these compounds that are armed with rich functionality allowing them to be chemoselectively derivatized with high diastereocontrol.

POLYMERIZATION OF OLEFINS

-

, (2008/06/13)

Olefins containing selected functional groups such as silyl, ether and alkenyl, and often containing a blocking group, may be copolymerized with unsubstituted olefins such as ethylene and propylene in the presence of certain coordination compounds of nickel or palladium. The resulting polymers are useful as molding resins, elastomers, in adhesives and for films.

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