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Cas:6757-06-8
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inquiryItems Standard Result Assay (Ursolic acid) 98%min 98.22% --------------------------------------------------------------------------------------
Cas:6757-06-8
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inquiryHigh quality Cytidine 5'-monophosphate disodium salt CAS 6757-06-8 in stock Company profile Wuhan Fortuna Chemical Co.,Ltd established in 2006, is a big integrative chemical enterprise being engaged in Pharmaceutical & its intermediates,
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inquiryTIANFUCHEM-- 6757-06-8--Cytidine 5'-monophosphate disodium salt factory price Our company was built in 2009 with an ISO certificate.In the past 10 years, we have grown up as a famous fine chemicals supplier in China And we had establis
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inquiryCytidine 5'-monophosphate disodium salt Basic information Product Name: Cytidine 5'-monophosphate disodium salt Synonyms: 5'-CMP 2NA;5'-CYTIDYLIC ACID DISODIUM SALT;CYTIDYLIC ACID DISODIUM SALT;CYTIDINE-5'-MONOPHOSPHATE
Cas:6757-06-8
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inquiryWith our good experience, we offer detailed technical support and advice to assist customers. We communicate closely with customers to establish their quality requirements. Consistent Quality Our plant has strict quality control in each manufacturin
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inquiryProduction name Cytidine 5'-monophosphate disodium salt CAS No. 6757-06-8 Appearance White powder Molecular Formula C9H12N3Na2O8P Molecular Weight 367.16 Assay 99% Appe
Cas:6757-06-8
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Cas:6757-06-8
Min.Order:10 Gram
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Cas:6757-06-8
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Min.Order:10 Gram
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inquiryTrade Assurance Get full protection for your orders 100% Product quality protection 100% On-time shipment protection 100% Payment protection Appearance:white crystalline powder Storage:Store in tight containers, in a cool dry place(2-8°C) Package:
Cas:6757-06-8
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inquiryProduct Name: Cytidine 5'-monophosphate disodium salt Synonyms: CYTIDINE-5'-MONOPHOSPHATE DISODIUM SALT(SH);disodium cytidine 5'-monophosphate;Cytidine-5'monohposphate Disodium Salt;Cytidine-5'-Monophosphoric Acid Disodium Sa
Cas:6757-06-8
Min.Order:100 Gram
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inquirySuperior quality, moderate price & quick delivery. Appearance:white powder Storage:Stored in cool, dry and ventilation place; Away from fire and heat Package:10g/bag,or as your request Application:Used as Pharmaceutical Intermediates Transp
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inquirycytidine-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; |
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