cytidine-5'-monophosphate disodium salt
Conditions | Yield |
---|---|
With water; zinc(II) cation pH=5.5; |
Conditions | Yield |
---|---|
In ethanol at 40℃; | 76% |
Conditions | Yield |
---|---|
In methanol for 0.5h; pH=4; | 75% |
cytidine-5'-monophosphate disodium salt
water
trans-1,2-bis(4-pyridyl)ethylene
Conditions | Yield |
---|---|
Stage #1: cobalt(II) nitrate hexahydrate; cytidine-5'-monophosphate disodium salt; water for 0.5h; Stage #2: trans-1,2-bis(4-pyridyl)ethylene With nitric acid In ethanol at 20℃; for 0.5h; pH=5; | 72% |
cytidine-5'-monophosphate disodium salt
water
trans-1,2-bis(4-pyridyl)ethylene
Conditions | Yield |
---|---|
Stage #1: manganese(II) perchlorate hexahydrate; cytidine-5'-monophosphate disodium salt; water for 0.5h; Stage #2: trans-1,2-bis(4-pyridyl)ethylene With sodium hydroxide In ethanol at 20℃; for 0.5h; pH=6; | 68% |
cytidine-5'-monophosphate disodium salt
water
trans-1,2-bis(4-pyridyl)ethylene
Conditions | Yield |
---|---|
Stage #1: manganese(II) perchlorate hexahydrate; cytidine-5'-monophosphate disodium salt; water for 0.5h; Stage #2: trans-1,2-bis(4-pyridyl)ethylene With sodium hydroxide In ethanol at 20℃; for 0.5h; pH=7; | 68% |
cytidine-5'-monophosphate disodium salt
Conditions | Yield |
---|---|
With 3-chloro-benzenecarboperoxoic acid In methanol at 0 - 20℃; for 24.25h; | 42% |
cytidine-5'-monophosphate disodium salt
Conditions | Yield |
---|---|
In water soln. of nucleotide (pH=7) is added dropwise to a soln. of amino acid chromium complex, soln. is placed in a thermostated bath at 50°C with const. stirring for 8 h; soln. is concd. to 5 ml, chromy. (Sephadex), addn. of ethanol to the first (blue) fraction, further evapn., ppt. is vac. dried (P4O10); elem. anal.; |
cytidine-5'-monophosphate disodium salt
Conditions | Yield |
---|---|
In water soln. of nucleotide (pH approx. 7) is added dropwise to a soln. of amino acid chromium complex (pH 3.9-4.2), mixt. is maintained at 50°C with const. stirring for 1.5-2.5 h; ppt. is filtered off, washed with cold water and vac. dried (P4O10); elem. anal.; |
trans-{CrCl2(C2H4(NH2)2)2}Cl
cytidine-5'-monophosphate disodium salt
Conditions | Yield |
---|---|
In water aq. soln. of Cr compd. mixed with aq. soln. of org. compd. (mole ratio Cr : org. compd. = 1 : 1); soln. heated at ca. 55 °C for 5-7 h; soln. concd. at 50 °C and passed through a colomn; ethanol addedto eluate; resulting ppt. filtered, washed (EtOH), and dried over silica gel; elem. anal.; |
cytidine-5'-monophosphate disodium salt
Conditions | Yield |
---|---|
In water aq. soln. of Cr compd. mixed with aq. soln. of org. compd. (mole ratio Cr : org. compd. = 1 : 1); soln. heated at ca. 55 °C for 5-7 h; soln. concd. at 50 °C and passed through a colomn; ethanol addedto eluate; resulting ppt. filtered, washed (EtOH), and dried over silica gel; elem. anal.; |
pentaaminechlorocobalt(III) dichloride
cytidine-5'-monophosphate disodium salt
Conditions | Yield |
---|---|
With H2O; HClO4 In water Co-compd. (1 mmol) was dissolved in the min. amt. of H2O and 1 mmol of org. compd. in H2O; both solns. were mixed and brought to pH 4.5 by means of HClO4; the resulting soln. was concd. at 70°C for 5 min, then heated at 50°C for 20 h;; column chromy., the first fraction was pptd. with EtOH; the complex waswashed with ethanol and dried over P4O10; elem. anal.;; |
trans-dichlorobis(ethylenediamine)cobalt(III) chloride
cytidine-5'-monophosphate disodium salt
Conditions | Yield |
---|---|
With H2O In water Co-compd. (0.5 mmol) was dissolved in H2O and 1 mmol of org. compd. in H2O; both solns. were mixed and heated at 50°C with const. stirring for about 7 h;; column chromy., the first fraction was pptd. with EtOH; the complex waswashed with ethanol and dried over P4O10; elem. anal.;; |
cytidine-5'-monophosphate disodium salt
Conditions | Yield |
---|---|
With H2O In water pH 7.23, 310 K, 3 d; reaction was monitored by (1)H and (31)P NMR spectroscopy; (1)H and (31)P NMR data; |
deuteriated sodium hydroxide
cytidine-5'-monophosphate disodium salt
Conditions | Yield |
---|---|
In water; water-d2 concd. NaOD soln. added to stirred suspn. of Na salt of nucleotide and UO2(NO2)2*6H2O in H2O-D2O; pH 8.5-12; not isoalted; detd. by NMR spectra; two UO2 complexes obtained in soln.; | |
In water-d2 concd. NaOD soln. added to stirred suspn. of Na salt of nucleotide and UO2(NO2)2*6H2O in D2O; pH 8.5-12; not isoalted; detd. by NMR spectra; two UO2 complexes obtained in soln.; |
cytidine-5'-monophosphate disodium salt
Conditions | Yield |
---|---|
With potassium nitrate In water (N2); mixing cobalt complex and AMP in 0.2 M aq. KNO3 at pH 7.0; not isolated, detected by UV; |
cytidine-5'-monophosphate disodium salt
Conditions | Yield |
---|---|
With potassium nitrate In water (N2); mixing cobalt complex and AMP in 0.2 M aq. KNO3 at pH 7.0; not isolated, detected by UV; |
cytidine-5'-monophosphate disodium salt
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1.1: triethylamine / acetonitrile / 0.18 h / 0 - 20 °C / Inert atmosphere 2.1: triethylamine / acetonitrile / 0.17 h / 0 °C / Inert atmosphere 3.1: N,N-dimethyl-formamide / Molecular sieve; Inert atmosphere 3.2: Dowex-50-W ion-exchange resin, Na+ form View Scheme |
cytidine-5'-monophosphate disodium salt
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: triethylamine / acetonitrile / 0.18 h / 0 - 20 °C / Inert atmosphere 2: triethylamine / acetonitrile / 0.17 h / 0 °C / Inert atmosphere View Scheme |
cytidine-5'-monophosphate disodium salt
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1.1: triethylamine / acetonitrile / 0.18 h / 0 - 20 °C / Inert atmosphere 2.1: triethylamine / acetonitrile / 0.17 h / 0 °C / Inert atmosphere 3.1: N,N-dimethyl-formamide / Molecular sieve; Inert atmosphere 3.2: Dowex-50-W ion-exchange resin, Na+ form View Scheme |
cytidine-5'-monophosphate disodium salt
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1.1: triethylamine / acetonitrile / 0.18 h / 0 - 20 °C / Inert atmosphere 2.1: triethylamine / acetonitrile / 0.17 h / 0 °C / Inert atmosphere 3.1: N,N-dimethyl-formamide / Molecular sieve; Inert atmosphere 3.2: Dowex-50-W ion-exchange resin, Na+ form View Scheme |
Conditions | Yield |
---|---|
With triethylamine In acetonitrile at 0 - 20℃; for 0.183333h; Inert atmosphere; |
Molecular Structure of Cytidine 5'-monophosphate disodium salt (CAS NO.6757-06-8):
IUPAC Name: disodium [(2R,3S,4R,5R)-5-(4-amino-2-oxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methyl phosphate
Empirical Formula: C9H12N3Na2O8P
Molecular Weight: 367.1602
H bond acceptors: 11
H bond donors: 4
Freely Rotating Bonds: 10
Polar Surface Area: 162.95Å2
EINECS: 229-819-3
Melting point: 300 °C
Product Categories: Amino Acids;Biochemistry;Nucleosides, Nucleotides & Related Reagents;Nucleotides and their analogs;Nucleic acids
InChI
InChI=1/C9H14N3O8P.2Na/c10-5-1-2-12(9(15)11-5)8-7(14)6(13)4(20-8)3-19-21(16,17)18;;/h1-2,4,6-8,13-14H,3H2,(H2,10,11,15)(H2,16,17,18);;/q;2*+1/p-2/t4-,6-,7-,8-;;/m1../s1
Smiles
n1([C@H]2[C@@H]([C@H](O)[C@H](O2)COP(=O)([O-])[O-])O)c(nc(cc1)N)=O.[Na+].[Na+]
Hazard Codes: Xn,Xi
Risk Statements: 20/21/22-36/37/38
R20/21/22:Harmful by inhalation, in contact with skin and if swallowed.
R36/37/38:Irritating to eyes, respiratory system and skin.
Safety Statements: 22-24/25-37/39-36-26
S22:Do not breathe dust.
S24/25:Avoid contact with skin and eyes.
S37/39:Wear suitable gloves and eye/face protection.
S36:Wear suitable protective clothing.
S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
WGK Germany: 3
F: 1-10
Cytidine 5'-monophosphate disodium salt , with CAS number of 6757-06-8, can be called 5'-CMP disodium salt ; CMP disodium salt ; Cytidine 5'MP, disodium salt ; Cytidine monophosphate disodium salt ; Disodium 5'-CMP ; Disodium CMP ; Disodium cytidine 5'-monophosphate ; Disodium cytidine 5'-phosphate . It is a white crystalline powder.
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