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Cas:2731-06-8
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inquiry2-Methylindole-3-ethylamine CAS No.:2731-06-8 Name: 2-Methylindole-3-ethylamine Synonyms: 2-(2-Methyl-1H-indol-3-yl)-ethylamine; 3-(2-Aminoethyl)-2-methylindole Molecular Structure Molecul
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inquiryProduct Name: 2-Methylindole-3-ethylamine Synonyms: 3-(2-AMINOETHYL)-2-METHYLINDOLE;2-(2-METHYL-1H-INDOL-3-YL)ETHANAMINE;2-(2-METHYL-1H-INDOL-3-YL)-ETHYLAMINE;AKOS B006949;RARECHEM AN KA 1106;2-methyl-1H-indole-3-ethylamine;1H-Indole-2-Methyl-3-Et
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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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inquiryAdvantage : LIDE PHARMACEUTICALS LTD. is a mid-small manufacturing-type enterprise, engaged in pharmaceutical intermediates of R&D, custom-made and production, and also involving trading chemicals for export. We have established the R&
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Min.Order:1 Gram
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inquiry2-Methylindole-3-ethylamine CAS:2731-06-8 Qingdao Belugas Import and Export Co., Ltd. is a scientific and technological company integrating research and development, production and trade of chemical intermediates, specializing in high quality organ
Cas:2731-06-8
Min.Order:1 Gram
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inquiryHello, dear friend! I'm Hansen and Allen from China. Welcome to my lookchem mall! The following is a brief introduction of our company's products and services. If you are interested in our products, please contact us by emai
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Min.Order:10 Kilogram
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inquiryHenan Wentao Chemical Product Co.,Ltd is Located in Zhengzhou High-tech Development Zone with import and export license, We passed ISO 9001:2008 as well, Henan Wentao has developed more than 1000 compounds, which are widely used in the fields of prod
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inquiryLorcaserin(856681-05-5)is an orally administered agent and a selective 5-HT2C receptor agonist for the treatment of obesity. It had been approved for marketing in US by FDA on 27 June in 2012. In clinical studies, lorcaserin h
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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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inquiryMassive Chemical is certified with ISO9001 and ISO14001 manufacturer for this product. We will offer all documents as requirement for the materials which includes, Certificate of Analysis, Material Safety Data Sheet, and Method of Analysis and
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Min.Order:1 Gram
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inquiryHuarong Industrial Group Limited established since 2006 , has been actively developing specialty products for Finished Dosages, APIs, Intermediates, and Fine chemicals markets in North America, Europe, Korea, Japan, Mid-East and all over the World.
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Min.Order:1 Gram
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Type:Trading Company
inquiryProduct Details Grade: pharmaceutical grade Purity:99%+ ProductionCapacity: 1000 Kilogram/Month Scope of use: For scientific research only(The product must be used legally) Our Advantage 1. Best quality with competitive price. 2. Quick shipping,
Cas:2731-06-8
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inquiryProduct Name: 2-Methylindole-3-ethylamine Synonyms: ART-CHEM-BB B006949;2-Methylindole-3-ethylamine;2-METHYL TRYPTAMINE;3-(2-AMINOETHYL)-2-METHYLINDOLE;2-(2-methyl-1H-indol-3-yl)ethanamine 0.95oxalate;2-(2-METHYL-1H-INDOL-3-YL)ETHANAMINE;2-(2-M
Cas:2731-06-8
Min.Order:1 Gram
Negotiable
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inquiryfactory?direct?saleAppearance:White Powder Storage:Store In Dry, Cool And Ventilated Place Package:25kg/drum, also according to the clients requirement Application:It is widely used as a thickener, emulsifier and stabilizer Transportation:By Sea Or B
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Min.Order:1 Kilogram
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Type:Trading Company
inquiryShandong Mopai Biotechnology Co., LTD is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality pharmaceuticals, intermediates, special chemicals and OLED intermediates and other fine chemicals. W
Cas:2731-06-8
Min.Order:1 Gram
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inquiry1.Applied in food field.it can improve the immune system and prolong life. 2.Appliedin cosmetic field.it can improve the skin care. 3.Applied in pharmaceutical field.it can treat various dieases. 4.Our product quality assurance will make our customer
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Type:Trading Company
inquirySAGECHEM is a chemical R&D, manufacturing and distribution company in China since 2009, including pharmaceutical intermediates, agrochemical, dyestuff intermediates, organosilicone, API and etc. We also offer a full range of services in custom synthe
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inquiryHigh quality,stable supply chain.Appearance:white/off-white or light yellow Storage:Store in cool and dry place, keep away from strong light and heat. Package:aluminum bottle,glass bottle,PTFE bottle,cardboard drum Application:This product can be use
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inquiryWe are a Union of chemistry in China, consists of chemists,engineers, laboratories,factories in China. We organize surplus capacity of R&D and production as well as custom synthesis for chemical products and chemical business project. We are supp
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Min.Order:1 Metric Ton
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Type:Trading Company
inquiry1, High quality with competitive price:2, Fast and safe delivery3.Excellent pre-sales and after-sales service4. Well-trained and professional technologist and sales with rich experience in the field for 5-10 yearsAppearance:see detailed specification
Lower price, sample is available,SDS test documents are available,large stock in warehouseAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:Fine chemical intermediates, used as the main raw material for the synthe
Cas:2731-06-8
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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
Jinhua huayi chemical co., ltd. is dedicated to the development, production and marketing of chemicals. On the basis of equality and mutual benefit, and under the principle of customer first, credit first, quality first, we are ready to join hands
Cas:2731-06-8
Min.Order:100 Gram
Negotiable
Type:Lab/Research institutions
inquiryConditions | Yield |
---|---|
In ethanol at 80℃; for 4h; | 82% |
In ethanol at 80℃; for 4h; | 80% |
In ethanol; water at 75 - 150℃; for 0.333333h; Microwave irradiation; | 76% |
N-(2-(2-methyl-1H-indol-3-yl)ethyl)acetamide
2-methyltryptamine
Conditions | Yield |
---|---|
With ammonium bromide; ethylenediamine at 100℃; for 7h; Microwave irradiation; | 78% |
2-methyltryptamine
Conditions | Yield |
---|---|
With triethylsilane In acetonitrile at 20 - 30℃; | 76.6% |
2,2,2-trifluoro-N-(2-(2-methyl-1H-indol-3-yl)ethyl)acetamide
2-methyltryptamine
Conditions | Yield |
---|---|
With water; potassium carbonate In methanol for 2h; Reflux; | 75% |
Cyclopropyl methyl ketone
phenylhydrazine
A
2-methyltryptamine
B
3-methyl-1-phenyl-1,4,5,6-tetrahydropyridazine
Conditions | Yield |
---|---|
With ammonium iodide In acetonitrile for 16h; Reflux; | A 49% B 34% |
indole
N-Acetyltryptamine
A
2-methyltryptamine
B
tris(1H-indol-3-yl)methane
D
6-<(o-aminophenyl)methyl>-5,11-dihydroindolo<3,2-b>carbazole
(2R,3'R)-2-(1H-Indol-3-yl)-2'-methyl-1,2,4',5'-tetrahydro-spiro[indole-3,3'-pyrrole]
(2S,3'R)-2-(1H-Indol-3-yl)-2'-methyl-1,2,4',5'-tetrahydro-spiro[indole-3,3'-pyrrole]
Conditions | Yield |
---|---|
With trichlorophosphate In acetonitrile for 0.25h; Mechanism; Product distribution; Heating; labelling experiments; | A 9.6% B 0.8% C n/a D 3.5% E n/a F n/a |
indole
N-Acetyltryptamine
A
2-methyltryptamine
B
tris(1H-indol-3-yl)methane
(2R,3'R)-2-(1H-Indol-3-yl)-2'-methyl-1,2,4',5'-tetrahydro-spiro[indole-3,3'-pyrrole]
(2S,3'R)-2-(1H-Indol-3-yl)-2'-methyl-1,2,4',5'-tetrahydro-spiro[indole-3,3'-pyrrole]
Conditions | Yield |
---|---|
With trichlorophosphate In acetonitrile for 0.25h; Heating; Further byproducts given. Yields of byproduct given; | A 9.6% B 0.8% C n/a D n/a |
With trichlorophosphate In acetonitrile for 0.25h; Heating; Yield given. Further byproducts given. Yields of byproduct given. Title compound not separated from byproducts; | A 9.6% B 0.8% C n/a D n/a |
Conditions | Yield |
---|---|
With ethanol; sodium |
2-Methyl-3-(2-nitroethyl)-1H-indole
2-methyltryptamine
Conditions | Yield |
---|---|
With ethanol; nickel Hydrogenation; | |
With hydrogen; palladium on activated charcoal In methanol for 0.5h; Ambient temperature; |
2-methyltryptamine
Conditions | Yield |
---|---|
With palladium; acetic acid Hydrogenation; |
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride | |
With lithium aluminium tetrahydride In tetrahydrofuran Heating; | |
With lithium aluminium tetrahydride In tetrahydrofuran at 0 - 20℃; for 4h; Heating / reflux; |
2-(1H-Indol-3-yl)-2'-methyl-1,2,4',5'-tetrahydro-spiro[indole-3,3'-pyrrole]
A
indole
B
2-methyltryptamine
Conditions | Yield |
---|---|
With hydrogenchloride for 0.5h; Yield given; |
α-methyl-β-(β-bromoethyl)indole
2-methyltryptamine
(E)-2-methyl-3-(2-nitrovinyl)-1H-indole
2-methyltryptamine
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride In tetrahydrofuran | |
Multi-step reaction with 2 steps 1: 94.5 percent / H2 / tris(triphenylphosphine)rhodium(I) chloride / benzene / 20 h / 50 °C / 7500.6 Torr 2: H2 / Pd/C / methanol / 0.5 h / Ambient temperature View Scheme | |
With lithium aluminium tetrahydride In tetrahydrofuran at 0 - 20℃; |
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: POCl3 2: AcOH 3: LiAH4 / tetrahydrofuran View Scheme | |
Multi-step reaction with 3 steps 1: diethyl ether / Heating 2: NH3 / dioxane 3: lithium aluminum hydride / tetrahydrofuran / Heating View Scheme | |
Multi-step reaction with 3 steps 1: 80.4 percent / CF3COOH / CH2Cl2 / 1) 0 deg C, 2.5 h, 2) rt, 20 h 2: 94.5 percent / H2 / tris(triphenylphosphine)rhodium(I) chloride / benzene / 20 h / 50 °C / 7500.6 Torr 3: H2 / Pd/C / methanol / 0.5 h / Ambient temperature View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: AcOH 2: LiAH4 / tetrahydrofuran View Scheme | |
Multi-step reaction with 3 steps 1: ammonium acetate 2: sodium tris(acetoxy)borohydride / tetrahydrofuran 3: palladium 10% on activated carbon; ammonium formate / methanol View Scheme | |
Multi-step reaction with 2 steps 1: ammonium acetate / 2 h / Reflux 2: lithium aluminium tetrahydride / tetrahydrofuran / 36 h / 0 - 20 °C / Inert atmosphere View Scheme | |
Multi-step reaction with 2 steps 1: ammonium acetate / 1.5 h / Reflux; Inert atmosphere 2: lithium aluminium tetrahydride / tetrahydrofuran / 36 h / 0 - 20 °C / Inert atmosphere View Scheme | |
Multi-step reaction with 2 steps 1: ammonium acetate / 3 h / 100 °C 2: lithium aluminium tetrahydride / tetrahydrofuran / 0 - 20 °C View Scheme |
(2-methyl-3-indolyl)glyoxyloyl chloride
2-methyltryptamine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: NH3 / dioxane 2: lithium aluminum hydride / tetrahydrofuran / Heating View Scheme | |
Multi-step reaction with 2 steps 1: aq.NH3 2: LiAlH4 View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 2: aq.NH3 3: LiAlH4 View Scheme |
Desoxy-dinor-9-methyl-eserolin
2-methyltryptamine
Conditions | Yield |
---|---|
In ethanol at 20℃; Reflux; |
α-methyl-β-(β-bromoethyl)indole
2-methyltryptamine
Conditions | Yield |
---|---|
Stage #1: α-methyl-β-(β-bromoethyl)indole With potassium phtalimide Stage #2: With hydrazine |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: sodium tris(acetoxy)borohydride / tetrahydrofuran 2: palladium 10% on activated carbon; ammonium formate / methanol View Scheme | |
With lithium aluminium tetrahydride In tetrahydrofuran at 0 - 20℃; for 36h; Inert atmosphere; | |
With lithium aluminium tetrahydride In tetrahydrofuran at 0 - 20℃; for 36h; Inert atmosphere; |
2-methyltryptamine
Conditions | Yield |
---|---|
With palladium 10% on activated carbon; ammonium formate In methanol |
2-chloro-1-(2-methyl-1H-indol-3-yl)ethan-1-one
2-methyltryptamine
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: N,N-dimethyl-formamide / 2 h / 85 °C 2: methylamine / ethanol; water / 2 h / 85 °C 3: triethylsilane / acetonitrile / 20 - 30 °C View Scheme |
2-methyltryptamine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: methylamine / ethanol; water / 2 h / 85 °C 2: triethylsilane / acetonitrile / 20 - 30 °C View Scheme |
2-methyltryptamine
Conditions | Yield |
---|---|
With Ruminococcus gnavus L-tryptophan decarboxylase In aq. phosphate buffer for 4h; pH=8.0; Catalytic behavior; Enzymatic reaction; |
Conditions | Yield |
---|---|
In ethanol | 95% |
2-methyltryptamine
methyl (2E)-3-(4-formylphenyl)acrylate
(E)-3-[4-[[2-(2-methyl-1H-indol-3-yl)ethylamino]methyl]phenyl]acrylic acid methyl ester hydrochloride
Conditions | Yield |
---|---|
Stage #1: 2-methyltryptamine; methyl (2E)-3-(4-formylphenyl)acrylate In methanol at 25 - 35℃; for 1h; Stage #2: With hydrogenchloride In ethanol; water at 0 - 5℃; for 1h; pH=3 - 4; Solvent; Temperature; | 90.4% |
Stage #1: 2-methyltryptamine; methyl (2E)-3-(4-formylphenyl)acrylate With sodium tetrahydroborate In methanol at 0℃; Stage #2: With hydrogenchloride In water |
2-methyltryptamine
di-tert-butyl dicarbonate
Conditions | Yield |
---|---|
In 1,4-dioxane at 20℃; for 16h; | 90% |
With sodium hydroxide In dichloromethane; ethyl acetate at 0 - 20℃; for 0.5h; |
2-methyltryptamine
isoalantolactone
(11R)-13-(2-methyltryptamino)-11,13-dihydroisoalantolactone ((3R,3aR,4aR,8aR,9aR)-3-{[2-(2-methyl-1H-indol-3-yl)ethylamino]methyl}-8a-methyl-5-methylidenedecahydronaphtho[2,3-b]furan-2-one)
Conditions | Yield |
---|---|
In methanol at 20℃; Michael Addition; | 83% |
Conditions | Yield |
---|---|
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane; N,N-dimethyl-formamide at 20℃; for 10h; | 83% |
2-methyltryptamine
(E)-p-formylcinnamic acid
(E)-3-(4-(((2-(2-methyl-1H-indol-3-yl)ethyl)amino)methyl)phenyl)acrylic acid
Conditions | Yield |
---|---|
With sodium tris(acetoxy)borohydride; acetic acid In tetrahydrofuran; methanol; 1,2-dichloro-ethane | 81% |
With sodium cyanoborohydride; acetic acid In methanol | 70% |
With sodium cyanoborohydride; acetic acid In methanol |
2-methyltryptamine
(E)-3-(3,4-bis(2-hydroxyethoxy)phenyl)acrylic Acid
(E)-3-(3,4-bis(2-hydroxyethoxy)phenyl)-N-(2-(2-methyl-1H-indol-3-yl)ethyl)acrylamide
Conditions | Yield |
---|---|
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 20℃; for 8h; | 80% |
2-methyltryptamine
Conditions | Yield |
---|---|
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane; N,N-dimethyl-formamide at 20℃; for 10h; | 80% |
2-methyltryptamine
bis(trichloromethyl) carbonate
19-nor-Δ1,3,5(10)-22α-spirostatriene-3-ol
Conditions | Yield |
---|---|
Stage #1: bis(trichloromethyl) carbonate; 19-nor-Δ1,3,5(10)-22α-spirostatriene-3-ol With N-ethyl-N,N-diisopropylamine In dichloromethane at 0℃; for 0.5h; Inert atmosphere; Stage #2: 2-methyltryptamine In dichloromethane at 20℃; for 3h; Inert atmosphere; | 79% |
2-methyltryptamine
3-Bromobenzenesulfonyl chloride
3-bromo-N-[2-(2-methyl-1H-indol-3-yl)ethyl]benzenesulfonamide
Conditions | Yield |
---|---|
With pyridine In acetonitrile at 20℃; for 2h; Inert atmosphere; | 76% |
With pyridine In acetonitrile at 20℃; for 2h; Inert atmosphere; | 76% |
Conditions | Yield |
---|---|
With dmap In acetonitrile at 20℃; Inert atmosphere; Sealed tube; | 76% |
2-methyltryptamine
Conditions | Yield |
---|---|
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane; N,N-dimethyl-formamide at 20℃; for 10h; | 76% |
Conditions | Yield |
---|---|
Stage #1: styrylacetic acid With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 0℃; for 0.0833333h; Stage #2: 2-methyltryptamine In dichloromethane at 20℃; | 75% |
2-methyltryptamine
Conditions | Yield |
---|---|
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane; N,N-dimethyl-formamide at 20℃; for 10h; | 74% |
2-methyltryptamine
methyl 2,4-dioxopentanoate
methyl 4-formylbenzoate
methyl 4-(3-acetyl-4-hydroxy-1-(2-(2-methyl-1H-indol-3-yl)-ethyl)-5-oxo-2,5-dihydro-1H-pyrrol-2-yl)benzoate
Conditions | Yield |
---|---|
With pyridinium p-toluenesulfonate In 1,4-dioxane at 20℃; for 12h; | 73% |
Conditions | Yield |
---|---|
With sodium cyanoborohydride; acetic acid In methanol | 72% |
2-methyltryptamine
6-phenylpyridine-3-carboxylic acid
Conditions | Yield |
---|---|
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane; N,N-dimethyl-formamide at 20℃; for 10h; | 71% |
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane; N,N-dimethyl-formamide at 20℃; for 10h; | 71% |
2-methyltryptamine
4-(bromomethyl)benzaldehyde
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide at 20℃; for 3h; Temperature; Inert atmosphere; | 70% |
2-methyltryptamine
6-(2-fluorophenyl)pyridine-3-carboxylic acid
Conditions | Yield |
---|---|
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane; N,N-dimethyl-formamide at 20℃; for 10h; | 70% |
2-methyltryptamine
Methyl 3-formylbenzoate
Conditions | Yield |
---|---|
With sodium cyanoborohydride; acetic acid In methanol | 70% |
2-methyltryptamine
Conditions | Yield |
---|---|
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane; N,N-dimethyl-formamide at 20℃; for 10h; | 69% |
2-methyltryptamine
methyl 8-chloro-8-oxooctanoate
Conditions | Yield |
---|---|
With potassium carbonate In dichloromethane for 2h; | 68% |
2-methyltryptamine
Conditions | Yield |
---|---|
With sodium tris(acetoxy)borohydride; triethylamine In 1,2-dichloro-ethane at 20℃; for 15h; Inert atmosphere; | 68% |
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