Our company has been in existence for 10 years since its establishment. We have our own unique team. The company integrates independent research and development, production and sales. We have established famous brands at home and abroad. At present
Cas:124-02-7
Min.Order:1 Kilogram
FOB Price: $6.0 / 10.0
Type:Trading Company
inquiry
Cas:124-02-7
Min.Order:1 Metric Ton
FOB Price: $1.0
Type:Manufacturers
inquiryTIANFUCHEM--124-02-7--Diallylamine 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 established stable business relationsh
Cas:124-02-7
Min.Order:1 Metric Ton
FOB Price: $2000.0
Type:Lab/Research institutions
inquiryWITH US,YOUR MONEY IN SAFE,YOUR BUSINESS IN SAFE 1)Quick Response Within 12 hours; 2)Quality Guarantee: All products are strictly tested by our QC, confirmed by QA and approved by third party lab in China, USA, Canada, Germany, UK, Italy, France et
Cas:124-02-7
Min.Order:10 Gram
FOB Price: $146.0 / 176.0
Type:Trading Company
inquiryProduct Name Diallylamine CAS No. 124-02-7 MF C6H11N MW 97.16 Appearance:Colorless liquid Storage:Preserve in well-closed, light-resistant and airti
Cas:124-02-7
Min.Order:5 Metric Ton
FOB Price: $1.0 / 2.0
Type:Other
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 email in t
Cas:124-02-7
Min.Order:1 Kilogram
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inquiry1.In No Less 10 years exporting experience. you can 100% received goods 2.Lower Price with higher quality 3,Free sample 4,We are sincerely responsible for the "product quality" and "After Service" Upbio is Specializ
Cas:124-02-7
Min.Order:1 Gram
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Type:Lab/Research institutions
inquiryUsed in pharmaceutical intermediates, as well as intermediates for agricultural chemicals, dyes and coatings, organic synthesis and resin modifiers. It can also be used to prepare amphoteric polymers, organic synthetic materials, ionic water purifier
Henan 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
Cas:124-02-7
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Type:Lab/Research institutions
inquiryOur Advantage Rich Experience Our products are sold all over Europe,North&South America, Sino-East, Asia and pacific area as well as Africa,we establish long term. Quality service Company cooperates with research institutes. We strictly con
Cas:124-02-7
Min.Order:1 Kilogram
FOB Price: $1.0 / 10.0
Type:Trading Company
inquiryChemlyte Solutions believe that customers and suppliers deserve much more than what traditional distributors can offer. To grow in today s fast-paced and increasingly competitive market it is essential to be able to quickly adapt to market forces eff
Massive 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
Established in May 2015, TaiChem Ltd. is initially invested by a British research and development company and started by PhDs back from aboard. The company is registered in China Medical City (CMC), Taizhou, Jiangsu Province, and the production site
Zibo Hangyu Biotechnology Development 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 chemi
Cas:124-02-7
Min.Order:10 Gram
Negotiable
Type:Lab/Research institutions
inquiryProduct name: Diallylamine CAS No.:124-02-7 Molecule Formula:C6H11N Molecule Weight:97.15 Purity: 99% Package: 25kg/drum Description:Colorless to light yellow transparent liquid Manufacture Standards:Enterprise Standard TESTING I
Cas:124-02-7
Min.Order:1 Kilogram
Negotiable
Type:Lab/Research institutions
inquiryZhenyu biotech exported this product to many countries and regions at best price. if you are looking for the material's manufacturer or supplier in china, zhenyu biotech is your best choice. pls contact with us freely for getting detailed
Cas:124-02-7
Min.Order:1 Kilogram
FOB Price: $2.0
Type:Lab/Research institutions
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
Stock products, own laboratory Package:Grams, Kilograms Application:For R&D Transportation:According to customer request Port:Shanghai
Cas:124-02-7
Min.Order:0
Negotiable
Type:Lab/Research institutions
inquiryLower 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
TAIHO Unique Advantages:1.We're factory2.Free samples available3.Commodity inspection can be done4.ISO9001,Kosher certifications5.10 years experiences Storage:Store in cool &dry place Package:aluminium foil bag/fiber can/plastic drum Application:comp
J&H CHEM is one of China's leading providers of integrated fine chemical services including offering, research and development, Custom manufacturing business, as well as other Value-added customer services, for diversified range products of chemicals
high purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:Foil bag; Drum; Plastic bottle Application:Pharma;Industry;Agricultural Transportation:by sea or air Port:Beijing or Guangzhou
1.Factory supply with good quality and price.2.Regular order with good quality and price .3.ISO,Halal Koshert Certificate. 4.One biggest supplly in China.76.Factory offer.Appearance:colorless liquid Storage:store in a well-closed container away from
1. Best service, High quality and Reasonable price. 2. Customers can choose the packing way of produccts.. 3. Specials are possible when client's order is big enough, including the discount policy. 5. We can help our regular clients to su
factory?direct?sale Application:healing drugs
Cas:124-02-7
Min.Order:0
Negotiable
Type:Lab/Research institutions
inquirygood quality, competitive price, thoughtful after sale serviceAppearance:White to Off-White Solid Storage:Keep it in dry,shady and cool place Package:as your requirement Application:Pharma;Industry;Agricultural;chemical reaserch Transportation:by Sea
"HANGZHOU TIANYE CHEMICALS Co.LTD , Located in Eastern Science and Innovation Park Hangzhou .We are a high-tech enterprise specialized in technical research and development, production, development and trade of chemical products. We supply Multiple s
Trimeric sodium phosphate detergent auxiliary agent is a kind of excellent properties, is one of the biggest component of detergent consumption during the production, it has four aspects: 1, chelation of heavy metal ions, heavy metal ions in the wate
Best Seller, High Quality, Competitive Price, Fast Delivery, Quick ResponseAppearance:powder, or liquid Storage:Stored in room temperature, ventilated place Package:Bottle, barrel, cargo, container, etc. Application:Pharmaceuticals, intermediates, AP
1.Professional synthesis laboratory and production base. 2.Strong synthesis team and service team. 3.Professional data management system. 4.We provide the professional test date and product information ,ex. HNMR ,CNMR,FNMR, HPLC/G
Cas:124-02-7
Min.Order:10 Milligram
Negotiable
Type:Lab/Research institutions
inquiryA
5,7-Dimethoxy-2-phenylbenzofuran
B
diallylamine
Conditions | Yield |
---|---|
In benzene Irradiation; | A 96% B 56% |
diallylamine
Conditions | Yield |
---|---|
With samarium diiodide In tetrahydrofuran for 4h; Ambient temperature; | 90% |
N-butylamine
allyl alcohol
A
N-allyl-N-butylamine
B
diallylamine
Conditions | Yield |
---|---|
With ammonium hexafluorophosphate; [Pt(η3-C3H5)(DPP-Xantphos)]PF6 In toluene; acetonitrile at 30℃; for 44h; Inert atmosphere; | A 85% B 4% |
hexan-1-amine
allyl alcohol
A
N-allylhexan-1-amine
B
diallylamine
Conditions | Yield |
---|---|
With ammonium hexafluorophosphate; [Pt(η3-C3H5)(DPP-Xantphos)]PF6 In toluene; acetonitrile at 50℃; for 8h; Inert atmosphere; | A 81% B 7% |
Conditions | Yield |
---|---|
With ammonium hexafluorophosphate; [Pt(η3-C3H5)(DPP-Xantphos)]PF6 In toluene; acetonitrile at 30℃; for 20h; Inert atmosphere; | A 80% B 7% |
tert.-butyl lithium
A
(4,4-dimethylpent-1-en-2-yl)benzene
B
diallylamine
Conditions | Yield |
---|---|
Stage #1: N,N-diallyl-2-phenyl-2-propen-1-amine; tert.-butyl lithium In tetrahydrofuran at -78 - 0℃; Stage #2: With water In tetrahydrofuran | A n/a B 79% |
diallylamine
Conditions | Yield |
---|---|
Stage #1: N,N-diallyltritylamine With naphthalene; lithium In tetrahydrofuran at 0℃; for 6h; Stage #2: With water In tetrahydrofuran at 0 - 20℃; | 62% |
Conditions | Yield |
---|---|
With sulfuric acid | |
With sulfuric acid In water at 30℃; |
1,2-propanediene
1-amino-2-propene
A
Triallylamine
B
N-allyl(2,3-dimethylene)butylamine
C
Diallyl-(3-methyl-2-methylene-but-3-enyl)-amine
E
diallylamine
Conditions | Yield |
---|---|
sodium tetrahydroborate; triphenylphosphine; palladium dichloride at 150℃; for 1h; Product distribution; other temperatures, times; reaction with diallyl amine and N-allyl(2,3-dimethylene)butylamine; telomerization of propadiene with allyl amines; |
1,2-propanediene
1-amino-2-propene
A
N-allyl(2,3-dimethylene)butylamine
B
Diallyl-(3-methyl-2-methylene-but-3-enyl)-amine
D
diallylamine
Conditions | Yield |
---|---|
sodium tetrahydroborate; triphenylphosphine; palladium dichloride at 130℃; for 3h; |
1,2-propanediene
A
Diallyl-(3-methyl-2-methylene-but-3-enyl)-amine
B
diallylamine
Conditions | Yield |
---|---|
sodium tetrahydroborate; triphenylphosphine; palladium dichloride at 130℃; for 6h; |
diallylamine
Conditions | Yield |
---|---|
With sodium hydroxide 1.) CH2Cl2, -20 deg C, 10 min, 2.) room temperature, 30 min, 3.) 70 deg C, 1 h; Yield given. Multistep reaction; |
ammonia
3-chloroprop-1-ene
A
Triallylamine
B
1-amino-2-propene
C
diallylamine
Conditions | Yield |
---|---|
at 97 - 105℃; unter Druck; |
Conditions | Yield |
---|---|
With ammonia at 97 - 105℃; under 5884.06 - 11032.6 Torr; | |
With ammonia at 97 - 105℃; under 5884.06 - 11032.6 Torr; |
Conditions | Yield |
---|---|
With ammonia at 10℃; |
Conditions | Yield |
---|---|
Hydrolysis; |
Conditions | Yield |
---|---|
Hydrolysis; |
Conditions | Yield |
---|---|
With alkaline potassium hexacyanoferrate(III) In ethanol at 25℃; Mechanism; Rate constant; Kinetics; variations in the ionic strength of the reaction medium (cations and anions), varying amount of solvent; ΔG(excit.), ΔH(excit.), ΔS(excit.); |
benzyl diallylcarbamate
diallylamine
Conditions | Yield |
---|---|
With naphthalen-1-yl-lithium In tetrahydrofuran at 0℃; for 1h; | 62 % Chromat. |
3-chloroprop-1-ene
A
Triallylamine
B
1-amino-2-propene
C
diallylamine
Conditions | Yield |
---|---|
Stage #1: 3-chloroprop-1-ene With formaldehyd; ammonia In methanol; water at 40 - 70℃; for 6h; Stage #2: With hydroxyammonium sulfate; sulfuric acid In methanol; water at 40℃; for 0.5h; pH=0.8; Stage #3: With sodium hydroxide In methanol; water pH=12; Product distribution / selectivity; | |
Stage #1: 3-chloroprop-1-ene With ammonia In methanol; water at 40 - 70℃; for 6h; Stage #2: With hydroxyammonium sulfate; sulfuric acid In methanol; water at 40℃; for 0.5h; pH=0.8; Stage #3: With sodium hydroxide In methanol; water pH=12; Product distribution / selectivity; | |
With ammonium hydroxide at 35℃; for 0.666667h; Temperature; |
piperidine
C13H23NO
A
1-(piperidin-1-yl)heptan-1-one
B
diallylamine
Conditions | Yield |
---|---|
With Al2(NMe2)6 In toluene at 90℃; for 16h; Equilibrium constant; |
Conditions | Yield |
---|---|
With Al2(NMe2)6 In toluene at 90℃; for 16h; Equilibrium constant; |
1,2-propanediene
A
Triallylamine
B
1-amino-2-propene
C
diallylamine
Conditions | Yield |
---|---|
With AuC27H42N2(1+)*B(C6F5)4(1-)=(AuC27H42N2)(B(C6F5)4); ammonia In benzene-d6 at -60 - 165℃; Inert atmosphere; | |
With ammonia; AuC27H42N2(1+)*B(C6F5)4(1-)=(AuC27H42N2)(B(C6F5)4) In benzyl methyl ether; benzene-d6 at -60 - 175℃; Conversion of starting material; |
Conditions | Yield |
---|---|
With AuC27H42N2(1+)*B(C6F5)4(1-)=(AuC27H42N2)(B(C6F5)4); ammonia In benzene-d6 at -60 - 175℃; Inert atmosphere; |
Conditions | Yield |
---|---|
With rhodium(III) 5,10,15,20-tetra(p-sulfonatophenyl)porphyrin; oxygen; trifluoroacetic acid In water at 100℃; under 760.051 Torr; for 2h; |
diallylamine
Conditions | Yield |
---|---|
Stage #1: diphenyl diallylphosphoramidate With water; monoammonium para-toluenesulfonate; o-phthalic dicarboxaldehyde In acetonitrile at 90℃; for 24h; Sealed tube; Stage #2: With sodium hydroxide In water pH=8 - 9; chemoselective reaction; |
Conditions | Yield |
---|---|
In ethanol for 24h; Heating; | 100% |
In ethanol at 95℃; Sealed tube; | 100% |
With triethylaluminum 1.) toluene, CH2Cl2, 25-30 deg C, 30 min, 2.) room temperature; Yield given. Multistep reaction; |
C-phenyl-N-methylnitrone
diallylamine
Conditions | Yield |
---|---|
In chloroform at 60℃; for 72h; | 100% |
In chloroform at 60℃; for 72h; Cyclization; | 100% |
Conditions | Yield |
---|---|
Stage #1: diallylamine; ethyl trans-3-phenyl-1-oxirane-2-carboxylate In ethanol for 12h; Ring cleavage; addition; Heating; Stage #2: With methanesulfonyl chloride; triethylamine In dichloromethane at 0 - 20℃; for 3h; Rearrangement; chlorination; | 100% |
Cinnamyl acetate
diallylamine
(E)-N,N-diallyl-3-phenylprop-2-en-1-amine
Conditions | Yield |
---|---|
bis(η3-allyl-μ-chloropalladium(II)); (1RS,2RS,3SR,4SR)-1,2,3,4-tetrakis((diphenylphosphanyl)methyl)cyclopentane In water at 25℃; for 40h; | 100% |
bis(η3-allyl-μ-chloropalladium(II)); Tedicyp In water at 25℃; for 40h; | 99% |
bicyclo(3.2.0)hept-2-en-6-one
5-phenyl-[1,2,4]triazine-3-carboxylic acid ethyl ester
diallylamine
Conditions | Yield |
---|---|
With 4 A molecular sieve In chloroform for 21h; Heating; | 100% |
With 4 A molecular sieve In chloroform for 21h; Heating; | 100% |
cyclobutanone
5-phenyl-[1,2,4]triazine-3-carboxylic acid ethyl ester
diallylamine
Conditions | Yield |
---|---|
With 4 A molecular sieve In chloroform for 22h; Heating; | 100% |
With 4 A molecular sieve In chloroform for 22h; Heating; | 99% |
wortmannin
diallylamine
Conditions | Yield |
---|---|
In dichloromethane at 20℃; for 1h; | 100% |
In dichloromethane at 20℃; for 1h; | 68% |
diallylamine
(1R,2S,4S)-(+)-(N-bromoacetyl)bornane-10,2-sultam
(1R,2S)-N-[2'-(diallylamino)acetyl]bornane-10,2-sultam
Conditions | Yield |
---|---|
With potassium carbonate In acetone at 20℃; | 100% |
L-N-Boc-Ala
diallylamine
(S)-tert-butyl 1-(diallylamino)-1-oxopropan-2-ylcarbamate
Conditions | Yield |
---|---|
Stage #1: L-N-Boc-Ala With dicyclohexyl-carbodiimide In dichloromethane at 20℃; for 0.5h; Inert atmosphere; Stage #2: diallylamine In dichloromethane at 20℃; for 12h; Inert atmosphere; | 100% |
With dicyclohexyl-carbodiimide In dichloromethane at 20℃; for 12h; |
17-formylwortmannin
diallylamine
Conditions | Yield |
---|---|
In dichloromethane for 0.5h; | 100% |
Conditions | Yield |
---|---|
With triethylamine In acetonitrile at 20℃; for 1.5h; | 100% |
diallylamine
Trichloroacetyl chloride
N,N-diallyl-α,α,α-trichloroacetamide
Conditions | Yield |
---|---|
With pyridine In dichloromethane at 0 - 20℃; for 2h; | 100% |
With pyridine In dichloromethane at 20℃; for 2h; | 94% |
2,3-dihydro-2H-furan
carbon disulfide
diallylamine
tetrahydrofuran-2-yl diallylcarbamodithioate
Conditions | Yield |
---|---|
In water at 20℃; for 16h; regiospecific reaction; | 100% |
Conditions | Yield |
---|---|
Stage #1: oxalyl dichloride; Benzoylformic acid With copper diacetate; N,N-dimethyl-formamide In dichloromethane at 20℃; for 2h; Stage #2: diallylamine With triethylamine In dichloromethane | 100% |
Conditions | Yield |
---|---|
With dmap; triethylamine In 1,2-dichloro-ethane Reflux; Inert atmosphere; | 100% |
Conditions | Yield |
---|---|
In neat (no solvent) at 20℃; for 6h; Green chemistry; regioselective reaction; | 100% |
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 20℃; for 14h; Inert atmosphere; | 100% |
2-bromo-4-methoxybenzenesulfonyl chloride
diallylamine
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 0 - 20℃; for 15h; | 100% |
2-bromo-5-methoxybenzenesulfonyl chloride
diallylamine
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 0 - 20℃; for 15h; | 100% |
Conditions | Yield |
---|---|
In diethyl ether at 20℃; for 0.166667h; | 99% |
With 1,6-anhydro-3,4-dideoxy-β-D-glycero-hexopyranos-2-ulose at 0 - 20℃; for 1h; | 99% |
With triethylamine In dichloromethane at 0 - 20℃; for 1h; Inert atmosphere; | 95% |
Conditions | Yield |
---|---|
With triethylamine In benzene at 0℃; for 0.5h; | 99% |
With trimethylamine In ethyl acetate at 23℃; for 18h; Cooling with ice; | 75% |
With triethylamine In dichloromethane for 24h; Ambient temperature; | 71% |
Conditions | Yield |
---|---|
With 1,8-diazabicyclo[5.4.0]undec-7-ene In tetrahydrofuran at 0℃; Michael addition; | 99% |
With 1,8-diazabicyclo[5.4.0]undec-7-ene In tetrahydrofuran at -15℃; for 0.166667h; | 95% |
With 1,8-diazabicyclo[5.4.0]undec-7-ene In tetrahydrofuran at -15℃; for 0.666667h; |
Conditions | Yield |
---|---|
In methanol at 0 - 20℃; for 1h; | 99% |
With iodine at 20℃; for 0.5h; | 95% |
In cyclohexane at 20℃; for 20h; | 93% |
Conditions | Yield |
---|---|
Stage #1: 4-chlorobenzoyl chloride With pyridine; Merrifield's resin-bound 6-methyl-2-thiouracil In dichloromethane at 80℃; for 0.0833333h; microwave irradiation; Stage #2: diallylamine In dichloromethane at 80℃; for 0.0833333h; microwave irradiation; | 99% |
With triethylamine In dichloromethane at 0 - 20℃; for 1h; Inert atmosphere; | 97% |
With triethylamine In dichloromethane at 0 - 20℃; | 89% |
2-bromo-5-methoxy-benzoic acid
diallylamine
N,N-diallyl-2-bromo-5-methoxy-benzamide
Conditions | Yield |
---|---|
With dmap; dicyclohexyl-carbodiimide In dichloromethane at 0 - 20℃; | 99% |
Conditions | Yield |
---|---|
With 4C14H11NO3(2-)*2Ni(2+)*2Dy(3+)*2Cl(1-)*2C2H3N In acetonitrile at 20℃; for 24h; Reagent/catalyst; Molecular sieve; | 99% |
In water at 60℃; for 0.0833333h; Microwave irradiation; | 93% |
With 4 A molecular sieve; dysprosium(III) trifluoromethanesulfonate In acetonitrile at 20℃; for 16h; | 82% |
3-chloro-3-oxopropanoic acid methyl ester
diallylamine
methyl 3-(N,N-diallylamino)-3-oxopropanoate
Conditions | Yield |
---|---|
In dichloromethane at 10 - 20℃; | 99% |
di-tert-butyl dicarbonate
diallylamine
tert-butyl di(but-3-en-1-yl)carbamate
Conditions | Yield |
---|---|
In methanol at 0 - 20℃; | 99% |
rac-(E)-1,3-diphenyl-3-acetoxy-prop-1-ene
diallylamine
(S,E)-N,N-diallyl-(1,3-diphenyl-2-propenyl)amine
Conditions | Yield |
---|---|
With C32H31NO2PPd(1+)*F6P(1-); potassium acetate; N,O-bis-(trimethylsilyl)-acetamide at 20℃; for 4h; Inert atmosphere; Neat (no solvent); enantioselective reaction; | 99% |
With N,O-bis-(trimethylsilyl)-acetamide; bis(η3-allyl-μ-chloropalladium(II)); 1-benzyl-5-(((4R,5R)-2-(2-(diphenyl-phosphino)phenyl)-4,5-diphenyl-4,5-dihydro-1H-imidazol-1-yl)methyl)-1H-1,2,3-triazole; potassium acetate In dichloromethane for 24h; Inert atmosphere; Reflux; optical yield given as %ee; enantioselective reaction; |
Conditions | Yield |
---|---|
In neat (no solvent) at 35℃; for 1h; Solvent; Time; | 99% |
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