Substance
ID:181736
Names and Identifiers
Synonyms
α-(5,6-Dimethylbenzimidazolyl)cyanocobamideCyanocob(III)alamin氰钴胺维生素 B12CN-CblVitamin B12
IUPAC name
cyano[(1R,2R,3R,4R,6Z,8S,11Z,13S,14S,16Z,18S,19S)-8,13,18-tris(2-carbamoylethyl)-3,14,19-tris(carbamoylmethyl)-4-(2-{[(2R)-2-{[(2R,3S,4R)-5-(5,6-dimethyl-1H-1,3-benzodiazol-1-yl)-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl phosphonato]oxy}propyl]carbamoyl}ethyl)-1,4,6,9,9,14,16,19-octamethyl-20,21,22,23-tetraazapentacyclo[15.2.1.12,5.17,10.112,15]tricosa-5(23),6,10(22),11,15(21),16-hexaen-20-yl]cobaltylium
IUPAC Traditional name
cyano[(1R,2R,3R,4R,6Z,8S,11Z,13S,14S,16Z,18S,19S)-8,13,18-tris(2-carbamoylethyl)-3,14,19-tris(carbamoylmethyl)-4-(2-{[(2R)-2-{[(2R,3S,4R)-5-(5,6-dimethyl-1,3-benzodiazol-1-yl)-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl phosphonato]oxy}propyl]carbamoyl}ethyl)-1,4,6,9,9,14,16,19-octamethyl-20,21,22,23-tetraazapentacyclo[15.2.1.12,5.17,10.112,15]tricosa-5(23),6,10(22),11,15(21),16-hexaen-20-yl]cobaltylium
Registration numbers
EC Number
CAS Number
MDL Number
PubChem SID
Beilstein Number
Properties
Safety Information
Storage Temperature
2-8°C
German water hazard class
1
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
RTECS
GG3750000
Product Information
Purity
≥98%
Suitability
plant cell culture tested
Molecule Details
Biochem/physiol Actions
Cobalamin may be important to form organometallic bonds in nature and as a precursor of methylcobalamin. Methycobalamin is important for methionine biosynthesis and 5’-deoxyadenosyl cobalamin supports class II ribonucleotide reductase reactions.
Cobalamin may be important to form organometallic bonds in nature and as a precursor of methylcobalamin. Methycobalamin is important for methionine biosynthesis and 5’-deoxyadenosyl cobalamin supports class II ribonucleotide reductase reactions.
Molecular Spectra
No Data Available
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References
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