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701304-71-4

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701304-71-4 Usage

12-}\ textStructure{

H Contains a19 five\-membertextedNO heterocyclic \ ring)
witha Structure nitrogen atom: H.

-eter ocFunctionalyclic Groups compound with

a five-member Buteden ring containingyl group a ( nitrogen3 atom-b
uten-yl Functional)
Groups : -
Ethen yl group Buten (yl4 group-eth (enCyl)
4 -H Methyl7 group\ ())4 attached-m toethyl position )
1

Industrial Applications - E

then yl group (\ Syn(thesis ofC pharmaceutical2s
H 3 Production\ of)) ag attachedro tochemical position s4

Organic compound M synthesisethyl
group(\ (UsageCH:
3 ) attached Building block to position in organic4 synthesis

-Industrial Chemical intermediate Applications in: compound
production
-Synthesis Re ofactivity pharmaceutical:s Requires
further laboratory and Production industrial of ag research toro determinechemicals specific properties
and potential uses Formation of. other organic compounds

Potential Uses

Building block in organic synthesis
Chemical intermediate in compound production

Further Research

Properties characterization
Reactivity studies
Determination of specific applications through laboratory and industrial research

Check Digit Verification of cas no

The CAS Registry Mumber 701304-71-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,0,1,3,0 and 4 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 701304-71:
(8*7)+(7*0)+(6*1)+(5*3)+(4*0)+(3*4)+(2*7)+(1*1)=104
104 % 10 = 4
So 701304-71-4 is a valid CAS Registry Number.

701304-71-4Downstream Products

701304-71-4Relevant articles and documents

A concise synthesis of β-lactam-sulfonamide hybrids

Freitag, Dirk,Schwab, Pia,Metz, Peter

, p. 3589 - 3592 (2004)

Using ring closing metathesis (RCM) as the key operation, a rapid access to β-lactams fused to a sultam moiety of variable ring size was developed from low cost, commercially available starting materials. An efficient RCM of 4-vinyl-azetidin-2-ones to give 1-aza-bicyclo[4.2.0]oct-4-en-8-ones is also reported.

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