Faster access than browser!Similarities between Ethyl cyanohydroxyiminoacetate and Peptide synthesis
Ethyl cyanohydroxyiminoacetate and Peptide synthesis have 12 things in common (in Unionpedia): Acetic acid, Carbodiimide, Chemische Berichte, Dimethylformamide, Epimer, N,N'-Dicyclohexylcarbodiimide, N,N'-Diisopropylcarbodiimide, Nucleophile, Peptide synthesis, Racemization, Yield (chemistry), 1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide.
Acetic acid
Acetic acid, systematically named ethanoic acid, is a colourless liquid organic compound with the chemical formula CH3COOH (also written as CH3CO2H or C2H4O2).
Acetic acid and Ethyl cyanohydroxyiminoacetate · Acetic acid and Peptide synthesis ·
Carbodiimide
A carbodiimide or a methanediimine is a functional group consisting of the formula RN.
Carbodiimide and Ethyl cyanohydroxyiminoacetate · Carbodiimide and Peptide synthesis ·
Chemische Berichte
Chemische Berichte (usually abbreviated as Ber. or Chem. Ber.) was a German-language scientific journal of all disciplines of chemistry founded in 1868.
Chemische Berichte and Ethyl cyanohydroxyiminoacetate · Chemische Berichte and Peptide synthesis ·
Dimethylformamide
Dimethylformamide is an organic compound with the formula (CH3)2NC(O)H.
Dimethylformamide and Ethyl cyanohydroxyiminoacetate · Dimethylformamide and Peptide synthesis ·
Epimer
In stereochemistry, an epimer is one of a pair of stereoisomers.
Epimer and Ethyl cyanohydroxyiminoacetate · Epimer and Peptide synthesis ·
N,N'-Dicyclohexylcarbodiimide
N,N'-Dicyclohexylcarbodiimide is an organic compound with the chemical formula C13H22N2 whose primary use is to couple amino acids during artificial peptide synthesis.
Ethyl cyanohydroxyiminoacetate and N,N'-Dicyclohexylcarbodiimide · N,N'-Dicyclohexylcarbodiimide and Peptide synthesis ·
N,N'-Diisopropylcarbodiimide
N,N′-Diisopropylcarbodiimide is a carbodiimide used in peptide synthesis.
Ethyl cyanohydroxyiminoacetate and N,N'-Diisopropylcarbodiimide · N,N'-Diisopropylcarbodiimide and Peptide synthesis ·
Nucleophile
Nucleophile is a chemical species that donates an electron pair to an electrophile to form a chemical bond in relation to a reaction.
Ethyl cyanohydroxyiminoacetate and Nucleophile · Nucleophile and Peptide synthesis ·
Peptide synthesis
In organic chemistry, peptide synthesis is the production of peptides, compounds where multiple amino acids are linked via amide bonds, also known as peptide bonds.
Ethyl cyanohydroxyiminoacetate and Peptide synthesis · Peptide synthesis and Peptide synthesis ·
Racemization
In chemistry, racemization is the conversion of an enantiomerically pure mixture (one where only one enantiomer is present) into a mixture where more than one of the enantiomers are present.
Ethyl cyanohydroxyiminoacetate and Racemization · Peptide synthesis and Racemization ·
Yield (chemistry)
In chemistry, yield, also referred to as reaction yield, is the amount of product obtained in a chemical reaction.
Ethyl cyanohydroxyiminoacetate and Yield (chemistry) · Peptide synthesis and Yield (chemistry) ·
1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide
1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDC, EDAC or EDCI) is a water-soluble carbodiimide usually obtained as the hydrochloride.
1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide and Ethyl cyanohydroxyiminoacetate · 1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide and Peptide synthesis ·
The list above answers the following questions
- What Ethyl cyanohydroxyiminoacetate and Peptide synthesis have in common
- What are the similarities between Ethyl cyanohydroxyiminoacetate and Peptide synthesis
Ethyl cyanohydroxyiminoacetate and Peptide synthesis Comparison
Ethyl cyanohydroxyiminoacetate has 32 relations, while Peptide synthesis has 93. As they have in common 12, the Jaccard index is 9.60% = 12 / (32 + 93).
References
This article shows the relationship between Ethyl cyanohydroxyiminoacetate and Peptide synthesis. To access each article from which the information was extracted, please visit:
