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methyl 5-(furan-2-yl)penta-2,4-dienoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

23875-97-0

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23875-97-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23875-97-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,8,7 and 5 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 23875-97:
(7*2)+(6*3)+(5*8)+(4*7)+(3*5)+(2*9)+(1*7)=140
140 % 10 = 0
So 23875-97-0 is a valid CAS Registry Number.

23875-97-0SDS

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 methyl (2E,4E)-5-(furan-2-yl)penta-2,4-dienoate

1.2 Other means of identification

Product number -
Other names 5-furan-2-yl-penta-2,4-dienoic acid methyl ester

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:23875-97-0 SDS

23875-97-0Relevant academic research and scientific papers

Facile total synthesis of gymnoconjugatin A and B

Samala, Ramakrishna,Patro, Balaram,Basu, Manas K.,Kameswara Rao,Mukkanti

, p. 3624 - 3626 (2013)

A facile total synthesis of the microbial natural products gymnoconjugatin A and B, isolated from soil microbe of Gymnoascus reessii has been accomplished using inexpensive raw materials, furfural and trans-methyl crotonate using Horner-Wadsworth-Emmons (HWE) and Wittig reactions.

Synthesis and Properties of 5-Bromocycloheptafuran-4-one

Crabbe, Pierre,Depres, Jean-Pierre

, p. 2081 - 2083 (2007/10/02)

5-Bromocycloheptafuran-4-one reacted with ethylamine and isopropylamine to afford the corresponding 6-amino-derivatives by a cine-substitution reaction.The behaviour of this compound towards primary amines is different from that of the non-heteroaromatic analogue 6-bromobenzocyclohepten-5-one.

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