811842-25-8 Usage
General Description
L-4'-Tetrahydropyranyl glycine is a chemical compound that is a derivative of glycine, a naturally occurring amino acid in the human body. The addition of a tetrahydropyranyl group to glycine provides protection for the amino acid during chemical reactions and synthesis processes. This modification allows for the selective deprotection of the glycine molecule, making it a useful building block in organic synthesis and pharmaceutical development. L-4'-Tetrahydropyranyl glycine is often used in the production of peptide and protein-based drugs, as well as in the synthesis of complex organic molecules. It is an important chemical compound in the field of medicinal and pharmaceutical chemistry, providing a valuable tool for the creation of new drugs and therapeutics.
Check Digit Verification of cas no
The CAS Registry Mumber 811842-25-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,1,1,8,4 and 2 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 811842-25:
(8*8)+(7*1)+(6*1)+(5*8)+(4*4)+(3*2)+(2*2)+(1*5)=148
148 % 10 = 8
So 811842-25-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H13NO3/c8-6(7(9)10)5-1-3-11-4-2-5/h5-6H,1-4,8H2,(H,9,10)/t6-/m0/s1
811842-25-8Relevant articles and documents
SYNTHESIS METHOD FOR L-CYCLIC ALKYL AMINO ACID AND PHARMACEUTICAL COMPOSITION HAVING THEREOF
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Paragraph 0090; 0097, (2016/11/17)
A synthesis method for L-cyclic alkyl amino acid and a pharmaceutical composition having the said amino acid are provide in the present disclosure provides. The synthesis method comprises: step A.) preparing a cyclic alkyl keto acid or a cyclic alkyl keto acid salt having Structural Formula (I) or Structural Formula (II), and step B.) mixing the cyclic alkyl keto acid or the cyclic alkyl keto acid salt with ammonium formate, a leucine dehydrogenase, a formate dehydrogenase and a coenzyme NAD+, and carrying out a reductive amination reaction to generate the L-cyclic alkyl amino acid, wherein the Structural Formula (I) is where n1≧1, m1≧0 and the M1 is H or a monovalent cation; the Structural Formula (II) is where n2≧0, m2≧0, the M2 is H or a monovalent cation, an amino acid sequence of the leucine dehydrogenase is SEQ ID No.1.