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21080-92-2

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21080-92-2 Usage

Chemical Properties

white to light yellow crystal powder

Uses

3-Thiophenemalonic Acid (Ticarcillin EP Impurity C) is an intermediate used to synthesize temocillin. It is also used to prepare malonate-based inhibitors of mammalian serine racemase.

Check Digit Verification of cas no

The CAS Registry Mumber 21080-92-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,0,8 and 0 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 21080-92:
(7*2)+(6*1)+(5*0)+(4*8)+(3*0)+(2*9)+(1*2)=72
72 % 10 = 2
So 21080-92-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H6O4S/c8-6(9)5(7(10)11)4-1-2-12-3-4/h1-3,5H,(H,8,9)(H,10,11)/p-2

21080-92-2 Well-known Company Product Price

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  • (Code)Product description
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  • Detail
  • TCI America

  • (T1354)  3-Thiophenemalonic Acid  >98.0%(HPLC)(T)

  • 21080-92-2

  • 5g

  • 860.00CNY

  • Detail
  • TCI America

  • (T1354)  3-Thiophenemalonic Acid  >98.0%(HPLC)(T)

  • 21080-92-2

  • 25g

  • 2,250.00CNY

  • Detail
  • Aldrich

  • (215317)  3-Thiophenemalonicacid  97%

  • 21080-92-2

  • 215317-5G

  • 1,090.44CNY

  • Detail

21080-92-2Relevant articles and documents

Exploring the Promiscuous Enzymatic Activation of Unnatural Polyketide Extender Units in Vitro and in Vivo for Monensin Biosynthesis

Grote, Marius,Schulz, Frank

, p. 1183 - 1189 (2019/03/11)

The incorporation of new-to-nature extender units into polyketide synthesis is an important source for diversity yet is restricted by limited availability of suitably activated building blocks in vivo. We here describe a straightforward workflow for the biogenic activation of commercially available new-to-nature extender units. Firstly, the substrate scope of a highly flexible malonyl co-enzyme A synthetase from Streptomyces cinnamonensis was characterized. The results were matched by in vivo experiments in which the said extender units were accepted by both the polyketide synthase and the accessory enzymes of the monensin biosynthetic pathway. The experiments gave rise to a series of predictable monensin derivatives by the exploitation of the innate substrate promiscuity of an acyltransferase and downstream enzyme functions.

Process for producing 3-thienylmalonic acid

-

, (2008/06/13)

A process for preparing 3-thienyl malonic acid, comprising treatment of a 3-thienyl cyanoacetate of formula (III): STR1 where R1 represents an aryl or alkyl group, with at least a molar excess of an alkali metal hydroxide.

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