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127127-61-1

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127127-61-1 Usage

Properties

1. Chemical name: 2-Azetidinone, 4-(acetyloxy)-3-(1-methylethyl)-(3S-trans)-(9CI)
2. Molecular formula: C9H15NO3
3. Derivative of azetidinone
4. Contains an acetyloxy group
5. 3S-trans configuration
6. Potential applications in pharmaceuticals, organic synthesis, and industrial processes

Specific content

1. Chemical name: 2-Azetidinone, 4-(acetyloxy)-3-(1-methylethyl)-(3S-trans)-(9CI)
2. Molecular formula: C9H15NO3
3. Derived from azetidinone with a four-membered ring containing a nitrogen atom
4. Classified as an ester due to the acetyloxy group
5. 3S-trans configuration indicates stereochemistry
6. Potential applications in pharmaceuticals, organic synthesis, and industrial processes due to unique structure and properties
7. Further research and testing required for full understanding of potential uses and properties

Check Digit Verification of cas no

The CAS Registry Mumber 127127-61-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,1,2 and 7 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 127127-61:
(8*1)+(7*2)+(6*7)+(5*1)+(4*2)+(3*7)+(2*6)+(1*1)=111
111 % 10 = 1
So 127127-61-1 is a valid CAS Registry Number.

127127-61-1Downstream Products

127127-61-1Relevant articles and documents

The stereoselective preparation of mono- and bis-β-lactams by the 1,4-diaza 1,3-diene-acid chloride condensation: Scope and synthetic applications

Alcaide,Martin-Cantalejo,Perez-Castells,Rodriguez-Lopez,Sierra,Monge,Perez-Garcia

, p. 5921 - 5931 (2007/10/02)

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β-Lactams via α,β-Unsaturated Acid Chlorides: Intermediates for Carbapenem Antibiotics

Manhas, M. S.,Ghosh, Malay,Bose, Ajay K.

, p. 575 - 580 (2007/10/02)

Stereocontrolled synthesis of α-vinyl β-lactams and their transformation to convenient intermediates for PS-5, PS-6, asparenomycin, and thienamycin are described.

The α-Bromoester-Imine Condensation promoted by Zinc-Trimethylchlorosilane: A Stereospecific Short Formal Synthesis of (+/-)-Carbapenem Antibiotics and Realated Compounds

Cossio, Fernando P.,Odrizola, Jose M.,Oiarbide, Mikel,Palomo, Claudio

, p. 74 - 76 (2007/10/02)

Ethyl bromoacetate reacts with imines in the presence of zinc activated by trimethylchlorosilane to give high yields of 3-unsubstituted β-lactams.

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