111770-79-7

Basic information

• Product Name: N(4)-adenosyl-N(4)-methyl-2,4-diaminobutanoic acid
• Synonyms: N(4)-adenosyl-N(4)-methyl-2,4-diaminobutanoic acid
• CAS NO: 111770-79-7
• Molecular Formula: C15H23N7O5
• Molecular Weight: 381.38702
• Mol File: 111770-79-7.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 744.1°Cat760mmHg
• Flash Point: 403.8°C
• Appearance: /
• Density: 1.79g/cm³
• Vapor Pressure: 2.98E-23mmHg at 25°C
• Refractive Index: 1.784
• CAS DataBase Reference: N(4)-adenosyl-N(4)-methyl-2,4-diaminobutanoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: N(4)-adenosyl-N(4)-methyl-2,4-diaminobutanoic acid(111770-79-7)
• EPA Substance Registry System: N(4)-adenosyl-N(4)-methyl-2,4-diaminobutanoic acid(111770-79-7)

Safety Data

• Hazardous Substances Data: 111770-79-7(Hazardous Substances Data)

Usage

InChI:InChI=1/C15H23N7O5/c1-21(3-2-7(16)15(25)26)4-8-10(23)11(24)14(27-8)22-6-20-9-12(17)18-5-19-13(9)22/h5-8,10-11,14,23-24H,2-4,16H2,1H3,(H,25,26)(H2,17,18,19)/t7-,8+,10+,11+,14+/m0/s1

Upstream product

• 1355023-63-0 C₂₃H₃₅N₇O₇ 
• 34245-49-3 5'-deoxy-5'-methylamino-2',3'-O,O-(1-methylethylidene)adenosine 
• 5605-63-0 ((3aR,4R,6R,6aR)-6-(6-amino-9H-purin-9-yl)-2,2-dimethyl-tetrahydrofuro[3,4-d][1,3]dioxol-4-yl)methyl 4-methylbenzenesulfonate 
• 116701-00-9 methyl N⁴-(2',3'-O-isopropylidene-5'-adenosyl)-N⁴-methyl-2(R,S)-(trifluoroacetamido)-4-aminobutyrate 
• 116701-14-5 2-Amino-4-{[(3aR,4R,6R,6aR)-6-(6-amino-purin-9-yl)-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-ylmethyl]-methyl-amino}-butyric acid 
• 176847-64-6 (4S)-N-benzyloxycarbonyl-4-[2-[N-2',3'-O,O-(1-methylethylidene)adenosyl-N-methyl]aminoethyl]oxazolidin-5-one 

Relevant articles and documents

Homochiral synthesis of an aza analogue of S-adenosyl-L-methionine (AdoMet) and its binding to the E. coli methionine repressor protein (MetJ)

A synthesis of 5′-{N-[(S)-3-amino-3-carboxypropyl]-methylamino}-5′-deoxyadenosine from D-adenosine and (S)-glutamic acid is described; this product, AzaAdoMet 2, has a pKa of 7.10 for the tertiary amino group and so acts as a charge-switchable

Synthesis of Two Stable Nitrogen Analogues of S-Adenosyl-L-methionine

Homochiral syntheses of two stable nitrogen analogues of S-adenosyl-L-methionine (AdoMet) are described. In the first analogue, AzaAdoMet, the sulfonium center of AdoMet, is replaced by an N-methyl moiety whose pKa is 7.08. This provides a char