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inquiryHangzhou KeyingChem Co., Ltd. exported this product to many countries and regions at best price. If you are looking for the material’s manufacturer or supplier in China, KeyingChem is your best choice. Pls contact with us freely for getting det
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inquiryJ&H CHEM R&D center can offer custom synthesis according to the contract research and development services for the fine chemicals, pharmaceutical, biotechnique and some of the other chemicals. J&H CHEM has some Manufacturing base in Jia
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inquiryhigh purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:drum and bag Application:for pharma use Transportation:by sea or air Port:Beijing or Guangzhou
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inquiryAnsciep Chemical is a professional enterprise manufacturing and distributing fine chemicals and speciality chemicals. We have been dedicated to heterocycle compounds and phenyl rings for tens of years. This is our mature product for export. Our quali
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United Scientific Company Located in Shanghai of China , is a competitive player in the global specialty and fine chemical market. Fenghua has both the expertise and flexibility to produce a wide range of chemicals. Focusing on developing the innovat
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inquiryR & D enterprises have their own stock in stockAppearance:To be subject to the object Package:Customized Application:pharmaceutical intermediates Transportation:Air Port:Shanghai;Guangzhou
[1,1'-Biphenyl]-4,4'-diamine,hydrochloride (1:2) Storage:keep in dry and cool condition Package:25kg or according to cutomer's demand Application:Chemical research/pharma intermediate Transportation:By Sea,by Air,By courier like DHL or Fedx. Port:Sha
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inquiryHangzhou Keying Chem Co., Ltd. Is a comprehensive enterprise, dedicated to the development, production and marketing of chemicals. As a technology innovative and service professional enterprise, Our company mainly engages in global pharmaceutical, ch
Topbatt Chemical Co., Ltd., Established in 2019, located in Shenzhen, Guangdong Province, is a Manufacturer and Trading company which specialized in fine chemicals like Pharmaceutical Reference Standards and Stable Isotopes. Our Stable Isotopes produ
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Acidic organic/inorganic salts, such as Benzidine dihydrochloride, are generally soluble in water. The resulting solutions contain moderate to high concentrations of hydrogen ions and have pH's of less than 7.0. They react as acids to neutraliz
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inquiryN,N-dichloro-p-toluenesulfonamide
chloroform
diphenyl hydrazine
A
benzidine dihydrochloride
B
toluene-4-sulfonamide
C
trans-azobenzene
Conditions | Yield |
---|---|
With hydrogenchloride In water |
Conditions | Yield |
---|---|
In ethanol; water for 2h; Reflux; | 82% |
Conditions | Yield |
---|---|
Stage #1: benzidine dihydrochloride With hydrogenchloride; water; sodium nitrite at 0℃; Diazotization; Stage #2: azulene With sodium acetate In ethanol at 20℃; for 0.5h; Arylation; | 78% |
Stage #1: benzidine dihydrochloride With hydrogenchloride; water; sodium nitrite at 0℃; Diazotization; Stage #2: azulene With sodium acetate In ethanol at 20℃; for 0.5h; Arylation; Further stages.; | 78% |
benzidine dihydrochloride
5-hydroxy-3-methyl-1-(pyrid-2-yl)-1H-pyrazole
Conditions | Yield |
---|---|
Stage #1: benzidine dihydrochloride With hydrogenchloride; sodium nitrite In water at 0 - 5℃; Stage #2: 5-hydroxy-3-methyl-1-(pyrid-2-yl)-1H-pyrazole With sodium hydroxide; aluminium trichloride In water for 0.5h; pH=8.0 - 8.5; cooling; | 77% |
benzidine dihydrochloride
1-(4-chlorophenyl)-3-methyl-2-pyrazolin-5-one
Conditions | Yield |
---|---|
Stage #1: benzidine dihydrochloride With hydrogenchloride; sodium nitrite In water at 0 - 5℃; Stage #2: 1-(4-chlorophenyl)-3-methyl-2-pyrazolin-5-one With sodium hydroxide; aluminium trichloride In water for 0.5h; pH=8.0 - 8.5; cooling; | 76% |
benzidine dihydrochloride
1-(4-methoxyphenyl)-3-methyl-2-pyrazolin-5-one
Conditions | Yield |
---|---|
Stage #1: benzidine dihydrochloride With hydrogenchloride; sodium nitrite In water at 0 - 5℃; Stage #2: 1-(4-methoxyphenyl)-3-methyl-2-pyrazolin-5-one With sodium hydroxide; aluminium trichloride In water for 0.5h; pH=8.0 - 8.5; cooling; | 71% |
di-tert-butyl dicarbonate
benzidine dihydrochloride
Conditions | Yield |
---|---|
With 4-methyl-morpholine; dmap In 1,2-dimethoxyethane at 55℃; for 40h; | 64% |
Conditions | Yield |
---|---|
In methanol; water at 20℃; | 58% |
Conditions | Yield |
---|---|
In methanol excess of CdCl2 with 2 drops of concd.HCl in CH3OH added to soln. of ligand in CH3OH, stirred for 0.5 h; filtered, crystd., XRD; | 52% |
Conditions | Yield |
---|---|
With bromobenzene |
undec-10-enoyl chloride
benzidine dihydrochloride
Conditions | Yield |
---|---|
With diethyl ether; sodium carbonate |
Conditions | Yield |
---|---|
With triethylamine In 1,4-dioxane |
potassium cyanide
benzidine dihydrochloride
(1,1'-biphenyl)-4,4'-dicarbonitrile
Conditions | Yield |
---|---|
(i) aq. HCl, NaNO2, (ii) /BRN= 4652394/, aq. CuCN; Multistep reaction; |
benzidine dihydrochloride
4,4'-Bis-(phenyl-trans-azo)-biphenyl
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: bromobenzene 2: benzene / 140 °C / unter Druck View Scheme |
benzidine dihydrochloride
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: bromobenzene 2: bromobenzene View Scheme |
benzidine dihydrochloride
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: bromobenzene 2: bromobenzene View Scheme |
benzidine dihydrochloride
1,1'-(4,4'-biphenylene)bis(3-phenylurea)
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: bromobenzene 2: bromobenzene View Scheme |
benzidine dihydrochloride
N,N'-biphenyl-4,4'-diyl-bis-carbamic acid diphenyl ester
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: bromobenzene 2: bromobenzene View Scheme |
benzidine dihydrochloride
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: triethylamine / 1,4-dioxane 2: hydrogenchloride / ethyl acetate View Scheme |
benzidine dihydrochloride
4,4'-Bis-phenylglyoxyloyl-diphenyl
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: (i) aq. HCl, NaNO2, (ii) /BRN= 4652394/, aq. CuCN 2: (i) Mg, (ii) /BRN= 1869917/, (iii) aq. HCl 3: SeO2, Ac2O View Scheme |
benzidine dihydrochloride
4,4'-Bis-phenylacetyl-biphenyl
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: (i) aq. HCl, NaNO2, (ii) /BRN= 4652394/, aq. CuCN 2: (i) Mg, (ii) /BRN= 1869917/, (iii) aq. HCl View Scheme |
Conditions | Yield |
---|---|
In not given pptn. with H2SiF4 (D=1.30) from slightly hydrochloric soln. of benzidine hydrochloride at boiling temp.;; | >99 |
In not given pptn. with H2SiF4 (D=1.30) from slightly hydrochloric soln. of benzidine hydrochloride at boiling temp.;; | >99 |
benzidine dihydrochloride
Conditions | Yield |
---|---|
In hydrogenchloride at -15°C; in diluted HCl; | |
In hydrogenchloride at -15°C; in diluted HCl; |
tetracyanonickelate(II)
benzidine dihydrochloride
Conditions | Yield |
---|---|
In water pptn.;; | |
In water |
Conditions | Yield |
---|---|
In not given from hot soln. of calcd. amts. of educts; recrystn. from dild. HCl; |
Conditions | Yield |
---|---|
In water on dropping of a small amt. of PdCl2 soln. to a boiling soln. of base chloride in 1l H2O, immediately forming of sparingly sol. ppte.;; on washing with hot H2O and drying at 100 °C; it is difficult to obtain pure compd. because of sparing solubility of chloride of base;; | |
In ethanol on react. of alc. benzidine soln. with PdCl2 soln.;; |
Conditions | Yield |
---|---|
In hydrogenchloride mixt. of CdI2 and benzidine dichloride dissolved in H2O acidified by HCl; evapd. slowly; crystals isolated; |
Conditions | Yield |
---|---|
In hydrogenchloride mixt. of HgI2 and benzidine dichloride dissolved in H2O acidified by HCl; evapd. slowly; crystals isolated; |
α,α′,δ,δ′-tetramethylcucurbit[6]uril
benzidine dihydrochloride
Conditions | Yield |
---|---|
In water |
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