Conditions | Yield |
---|---|
With sodium hydroxide at 20℃; Sonication; | |
Stage #1: naphthalene-1,5-disulfonate With 4-nitro-2,6-dichloroaniline; sulfuric acid; cis-nitrous acid In 1,2-dimethoxyethane at 0 - 5℃; for 0.166667h; Stage #2: With sodium carbonate; m-acetylamino-N,N-diethylanilne In 1,2-dimethoxyethane at 0 - 40℃; for 0.5h; pH=6 - 8; |
disodium 1,5-naphthalenedisulfonate
Conditions | Yield |
---|---|
In dichloromethane; water at 20℃; | 94% |
In dichloromethane; water at 20℃; | 94% |
disodium 1,5-naphthalenedisulfonate
(S)-(+)-clopidogrel bisulfate
Conditions | Yield |
---|---|
In water; isopropyl alcohol at 5 - 70℃; for 17h; Product distribution / selectivity; | 94% |
In methanol; water at 5 - 70℃; for 17h; Product distribution / selectivity; | 94% |
In diethyl ether; water at 5 - 20℃; for 17h; Product distribution / selectivity; | 85% |
In water; toluene at 5 - 20℃; for 17h; Product distribution / selectivity; | 84% |
In water at 5 - 20℃; for 17h; Product distribution / selectivity; | 84% |
disodium 1,5-naphthalenedisulfonate
Conditions | Yield |
---|---|
In methanol; water at 5 - 60℃; for 17h; Product distribution / selectivity; | 94% |
In water; isopropyl alcohol at 5 - 70℃; for 17h; Product distribution / selectivity; | 86% |
disodium 1,5-naphthalenedisulfonate
Conditions | Yield |
---|---|
In water; isopropyl alcohol at 5 - 70℃; for 17h; Product distribution / selectivity; | 92% |
bis(1,1,1-tris(aminoethyl)ethane)cobalt(III) chloride
disodium 1,5-naphthalenedisulfonate
Conditions | Yield |
---|---|
In water ligand added to soln. of Co-complex in H2O, allowed to stand at 0°C for 12 h; ppt. filtered, washed with EtOH, Et2O; elem. anal. for dihydrate; | 91% |
disodium 1,5-naphthalenedisulfonate
Conditions | Yield |
---|---|
In water; isopropyl alcohol at 5 - 70℃; for 17h; Product distribution / selectivity; | 91% |
disodium 1,5-naphthalenedisulfonate
Conditions | Yield |
---|---|
In water; isopropyl alcohol at 5 - 70℃; for 17h; Product distribution / selectivity; | 88% |
In methanol; water at 5 - 20℃; for 17h; Product distribution / selectivity; | 85% |
disodium 1,5-naphthalenedisulfonate
Conditions | Yield |
---|---|
In water; isopropyl alcohol at 5 - 70℃; for 17h; Product distribution / selectivity; | 88% |
disodium 1,5-naphthalenedisulfonate
cadmium(II) acetate dihydrate
N,N`-dimethylethylenediamine
Conditions | Yield |
---|---|
In water 2 equiv. of N,N'-dimethylethylenediamine added with stirring to aq. soln. of Cd compd.; treated with 1 equiv. of sodium 1,5-naphthalenedisulfonate; crystd. over 4 d; elem. anal.; | 80% |
1H-imidazole
disodium 1,5-naphthalenedisulfonate
cadmium(II) acetate dihydrate
Conditions | Yield |
---|---|
In water disodium 1,5-naphthalenedisulfonate, imidazole added to aq. Cd(OAc)2; stirred for 4 h at 70°C; filtered; crystd. after 5 d; elem. anal.; | 80% |
[2-(4-chloro-benzyloxy)-ethyl]-[2-((R)-cyclohexylhydroxyphenylmethyl)-oxazol-5-ylmethyl]dimethylammonium bromide
disodium 1,5-naphthalenedisulfonate
Conditions | Yield |
---|---|
In dichloromethane; water at 20℃; for 1.16667h; Product distribution / selectivity; | 77% |
disodium 1,5-naphthalenedisulfonate
Conditions | Yield |
---|---|
With barium(II) chloride dihydrate; water In ethanol; N,N-dimethyl-formamide at 100℃; for 72h; High pressure; | 76% |
1,4-bis(imidazol-l-yl-methyl)benzene
disodium 1,5-naphthalenedisulfonate
cadmium(II) acetate
Conditions | Yield |
---|---|
With nitric acid; sodium hydroxide In water at 160℃; for 72h; pH=4.5; Autoclave; High pressure; | 75% |
Conditions | Yield |
---|---|
In water High Pressure; at 170°C under autogenous pressure for 66 h; cooled to ambient temp. in open air, decanted, washed (H2O), air-dried; elem. anal.; | 73% |
disodium 1,5-naphthalenedisulfonate
N,N`-dimethylethylenediamine
diaquabis(N,N'-dimethylethylenediamine)copper(II) 1,5-naphthalenedisulfonate monohydrate
Conditions | Yield |
---|---|
In water 2 equiv. of N,N'-dimethylethylenediamine added with stirring to aq. soln. of Cu salt; treated with 1 equiv. of Na2(C10H6(SO3)2); crystd. over 1 d; elem. anal.; | 72% |
2,4,5-tris(4-pyridinyl)imidazole
disodium 1,5-naphthalenedisulfonate
cadmium(II) acetate dihydrate
Conditions | Yield |
---|---|
In water at 180℃; for 72h; | 70% |
In water at 180℃; for 72h; Sealed tube; | 70% |
Conditions | Yield |
---|---|
In methanol at 95℃; for 48h; Activation energy; Sealed tube; | 70% |
disodium 1,5-naphthalenedisulfonate
N,N-dimethyl-formamide
Conditions | Yield |
---|---|
Stage #1: disodium 1,5-naphthalenedisulfonate With magnesium(II) chloride hexahydrate In ethanol; water at 20℃; for 2h; Stage #2: N,N-dimethyl-formamide | 67% |
Conditions | Yield |
---|---|
In methanol at 95℃; for 48h; Activation energy; Sealed tube; | 65% |
water
disodium 1,5-naphthalenedisulfonate
2,5-di(3-pyridylmethylidene)cyclopentanone
Conditions | Yield |
---|---|
Stage #1: water; disodium 1,5-naphthalenedisulfonate; silver nitrate; 2,5-di(3-pyridylmethylidene)cyclopentanone In methanol; N,N-dimethyl-formamide Stage #2: With ammonium hydroxide In methanol; N,N-dimethyl-formamide for 48h; | 64.23% |
water
disodium 1,5-naphthalenedisulfonate
2,2'-bis(4-pyridylmethylidene)cyclopentanone
Conditions | Yield |
---|---|
Stage #1: water; disodium 1,5-naphthalenedisulfonate; silver nitrate; 2,2'-bis(4-pyridylmethylidene)cyclopentanone In methanol; N,N-dimethyl-formamide Stage #2: With ammonium hydroxide In methanol; N,N-dimethyl-formamide for 48h; | 62.12% |
Conditions | Yield |
---|---|
In water High Pressure; at 170°C under autogenous pressure for 72 h; cooled to ambient temp. in open air, decanted, washed (H2O), air-dried; elem. anal.; | 56% |
water
disodium 1,5-naphthalenedisulfonate
2,6-di(3-pyridylmethylidene)cyclohexanone
Conditions | Yield |
---|---|
Stage #1: water; disodium 1,5-naphthalenedisulfonate; silver nitrate; 2,6-di(3-pyridylmethylidene)cyclohexanone In methanol; N,N-dimethyl-formamide for 48h; Stage #2: With ammonium hydroxide In methanol; N,N-dimethyl-formamide | 55.65% |
Conditions | Yield |
---|---|
With phosphorus pentachloride | 54% |
With pyridine; hydrogenchloride; phosphorus pentachloride 2.) 80 deg C, 5,5h; Yield given. Multistep reaction; |
Conditions | Yield |
---|---|
In water 2 equiv. of ethylenediamine added to aq. soln. of Cu salt; treated with 1 equiv. of Na2(C10H6(SO3)2); crystd. over 6 d; elem. anal.; | 52% |
disodium 1,5-naphthalenedisulfonate
1,2-diaminopropan
Conditions | Yield |
---|---|
In water 2 equiv. of 2,3-diaminopropane added with stirring to aq. soln. of Cu salt; treated with 1 equiv. of Na2(C10H6(SO3)2); crystd. over 1 d; elem. anal.; | 52% |
Conditions | Yield |
---|---|
at 120℃; for 72h; High pressure; | 43.1% |
Conditions | Yield |
---|---|
With uranyl nirate hexahydrate In 1-methyl-pyrrolidin-2-one; water at 140℃; for 168h; High pressure; | 40% |
1,4,8,11-Tetraazacyclotetradecane
disodium 1,5-naphthalenedisulfonate
(1,4,8,11-tetraazacyclotetradecane)copper(II) 1,5-naphthalenedisulfonate
Conditions | Yield |
---|---|
In methanol; water aq. soln. of Cu salt treated slowly with 1 equiv. of cyclam in MeOH withstirring; 1 equiv. of Na2(C10H6(SO3)2) dissolved in distd. water; cryst d. by slow diffusion of two solns. into U-tube contg. agar gel for 5 d; elem. anal.; | 10% |
Conditions | Yield |
---|---|
In water aq. soln. disodium naphthalene-1,5-disulfonate and CuCl2 (1:1 mol) was treated with tris(2-aminoethyl)amine (1 mol); room temp., 10 d; | 10% |
The 1,5-Naphthalenedisulfonicacid, sodium salt (1:2), with the cas registry number 1655-29-4, has its systematic name of disodium naphthalene-1,5-disulfonate. It product categories are including Intermediates of Dyes and Pigments. When store it, keep it at RT.
The characteristics of this chemical are as follows: (1)ACD/LogP: -0.05; (2)ACD/LogD (pH 5.5): -4.55; (3)ACD/LogD (pH 7.4): -4.55; (4)ACD/BCF (pH 5.5): 1; (5)ACD/BCF (pH 7.4): 1; (6)ACD/KOC (pH 5.5): 1; (7)ACD/KOC (pH 7.4): 1; (8)#H bond acceptors: 6; (9)#H bond donors: 2; (10)#Freely Rotating Bonds: 2; (11)Polar Surface Area: 125.5; (12)Exact Mass: 331.940119; (13)MonoIsotopic Mass: 331.940119; (14)Topological Polar Surface Area: 131; (15)Heavy Atom Count: 20; (16)Complexity: 423.
While dealing with this chemical, you should be very cautious. It is irritant and it may cause inflammation to the skin or other mucous membranes. Therefore, you should be careful. Do not breathe dust and avoid contacting with skin and eyes.
In addition, you could obtain the molecular structure by converting the following datas:
(1)SMILES:[Na+].[Na+].[O-]S(=O)(=O)c1cccc2c1cccc2S([O-])(=O)=O
(2)InChI:InChI=1/C10H8O6S2.2Na/c11-17(12,13)9-5-1-3-7-8(9)4-2-6-10(7)18(14,15)16;;/h1-6H,(H,11,12,13)(H,14,15,16);;/q;2*+1/p-2
(3)InChIKey:YGSZNSDQUQYJCY-NUQVWONBAJ
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