Puyang Huicheng Electronic Material Co., Ltd was founded in 2002, which is focus on high complex new type intermediates and fine chemical custom synthesis, LED&OLED materials and related intermediates, catalyst design and synthesis.
Cas:1462-03-9
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inquiryDayangchem's 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. DayangChem can provide different quantities
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inquiryWelcome to Simagchem, your partner in China as a premier supply of bulk specialty chemicals for industry and life science. We introduce experienced quality product and exceptional JIT service with instant market intelligence in China to benefit our
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inquiry1. Factory price and high quality must be guaranteed, base on 8 years of production and R&D experience2. Free samples will be provided,ensure specifications and quality are right for customer3. Customers will receive the most professional technical s
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inquiry
Cas:1462-03-9
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inquiry1-Methylcyclopentanol Basic information Product Name: 1-Methylcyclopentanol Synonyms: 1-Hydroxy-1-methylcyclopentane;1-Methyl-1-cyclopentanol;1-METHYLCYCLOPENTANOL;1-METHYLCYCLOPENTANOL,
Cas:1462-03-9
Min.Order:1 Gram
Negotiable
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:1462-03-9
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inquiry1-Methylcyclopentanol CAS No.: 1462-03-9 Formula: C6H12O Molecular weight: 100.16 Appearance: white crystalline low melting solid
Cas:1462-03-9
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inquiry1.High quality : the purity is 99% min . through multiple producing procedures. 2.Competitive price : low price because of our skilled production technolpgy ,save the production cost at most , and give big profit room to our customers 3.Safe a
1.No Less 8 years exporting experience. Clients 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 Specialized
Cas:1462-03-9
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inquiryProduct Name: 1-Methylcyclopentanol CAS: 1462-03-9 MF: C6H12O MW: 100.16 EINECS: 215-963-4 Mol File: 1462-03-9.mol 1-Methylcyclopentanol Structure 1-Methylcyclopentanol Chemical Properties Melting point 36-37 °C (lit.) Boi
Cas:1462-03-9
Min.Order:1 Gram
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inquiryOur 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:1462-03-9
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Type:Trading Company
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
Cas:1462-03-9
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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:1462-03-9
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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
Best quality & Attractive price & Professional service; Trial & Pilot & Commercial Hisunny Chemical is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality intermediates, specia
A substitute for perfluorooctanoic acid, mainly used as a surfactant, dispersant, additive, etc Appearance:White solid or Colorless liquid Purity:99.3 % We will ship the goods in a timely manner as required We can provide relevant documents acc
Cas:1462-03-9
Min.Order:4 Kilogram
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Type:Lab/Research institutions
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
Chemlyte 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
Cas:1462-03-9
Min.Order:100 Gram
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Type:Other
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
Cas:1462-03-9
Min.Order:1 Gram
FOB Price: $1.0
Type:Lab/Research institutions
inquirySuperior quality Appearance:white crystalline low melting solid Storage:Stored in cool, dry and ventilation place; Away from fire and heat Package:1kg/bag, 1kg/drum or 25kg/drum or as per your request. Application:Used as Pharmaceutical Intermediat
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
Cas:1462-03-9
Min.Order:10 Gram
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Type:Lab/Research institutions
inquiryThe above product is Ality Chemical's strong item with best price, good quality and fast supply. Ality Chemical has been focusing on the research and production of this field for over 14 years. At the same time, we are always committed to providing h
Product 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:1462-03-9
Min.Order:1 Kilogram
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Type:Lab/Research institutions
inquiryGMP standard, high purity, competitive price, in stock 1. Quick Response: within 6 hours after receiving your email. 2. Quality Guarantee: All products are strictly tested by our QC, confirmed by QA, and approved by a third-party lab in China, USA,
Hunan chemfish Pharmaceutical co.,Ltd.located in Lugu High-tech industral park ,Hunan province . with its own R&D center and more than 10000㎡manufacture plant . Chemfish owns 40 reactors from 1000L to 8000L. With complete auxiliary equipment as
Zhenyu 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:1462-03-9
Min.Order:1 Kilogram
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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
Cas:1462-03-9
Min.Order:1 Metric Ton
FOB Price: $7.0 / 8.0
Type:Trading Company
inquiryISO9001 Exporting Japan, Korea regularly. Appearance:Light yellow liquid Storage:Store in dry and cool place with good seal Package:25liter/200liter plastic drum Application:OLED intermediates Transportation:by courier,by Air,by Sea ... Port:Chin
Stock products, own laboratory Package:Grams, Kilograms Application:For R&D Transportation:According to customer request Port:Shanghai
Cas:1462-03-9
Min.Order:0
Negotiable
Type:Lab/Research institutions
inquirycyclopentanone
methyl iodide
A
1-methylcyclopentanol
B
bicyclopentyl-1,1'-diol
Conditions | Yield |
---|---|
With Pr 1.) THF, 20 deg C, 2.) -20 deg C; | A 86% B 2% |
Conditions | Yield |
---|---|
In diethyl ether for 48h; Ambient temperature; | 70% |
Conditions | Yield |
---|---|
With water; Amberlyst 15 In isopropyl alcohol at 55℃; | 39% |
With water; Amberlyst 15 In isopropyl alcohol at 55℃; for 0.8h; Product distribution / selectivity; | 39% |
acetonitrile
A
S-Phenyl benzenethiosulfonate
C
1-methylcyclopentanol
D
S-phenyl benzenethiosulfinate
E
N-(1-methylcyclopentyl)acetamide
F
diphenyldisulfane
Conditions | Yield |
---|---|
With titanium(IV) oxide; silver sulfate In water at 20℃; for 0.5h; Irradiation; | A n/a B 0.8% C 27.3% D n/a E 5.5% F n/a |
Conditions | Yield |
---|---|
With palladium 10% on activated carbon In diethyl ether; toluene at 0℃; Inert atmosphere; | 22% |
With diethyl ether |
methyl magnesium iodide
1-hydroxycyclopentanecarbonitrile
1-methylcyclopentanol
Conditions | Yield |
---|---|
With diethyl ether |
1-methyl-4-nitrosobenzene
1-methyl-cyclopentyl hydroperoxide
A
n-hexan-2-one
B
1-methylcyclopentanol
C
2-oxo-propionic acid
1-chloro-1-methylcyclopentane
A
1-methylcyclopent-1-ene
B
1-methylcyclopentanol
Conditions | Yield |
---|---|
With water In ethanol at 30℃; Rate constant; solvolysis reaction; | |
With calcium hydroxide; water at 35℃; |
1-methyl-cyclopentyl hydroperoxide
A
n-hexan-2-one
B
6-hydroxy-2-hexanone
C
1-methylcyclopentanol
Conditions | Yield |
---|---|
With magnesium Zerlegen der Magnesiumverbindung mit Wasser; | |
With magnesium 1.) ether, 2.) ether, from 0 deg C to reflux, 2 h; Yield given. Multistep reaction; | |
With lithium In tetrahydrofuran at 40 - 65℃; for 3h; Inert atmosphere; |
6-chloro-2-hexanone
1-methylcyclopentanol
Conditions | Yield |
---|---|
With amalgamated magnesium In tetrahydrofuran | |
Multi-step reaction with 2 steps 1: NaI / acetone 2: 21 percent Chromat. / tetrahydrofuran / -100 °C View Scheme | |
Multi-step reaction with 2 steps 1: NaI / acetone 2: 26 percent Chromat. / t-BuLi / diethyl ether / -78 °C / Var.: n-BuLi, THF, -100 deg C View Scheme |
6-Bromo-2-hexanone
1-methylcyclopentanol
Conditions | Yield |
---|---|
With amalgamated magnesium In tetrahydrofuran | |
With CuI*P(n-Bu)3; tributylphosphine; oxonium; naphthalen-1-yl-lithium 1. THF, -78 deg C, 20min; Yield given. Multistep reaction; |
n-butyllithium
1-iodo-5-hexanone
A
1-methylcyclopentanol
B
1-Iodo-5-methyl-nonan-5-ol
Conditions | Yield |
---|---|
In tetrahydrofuran at -100℃; Title compound not separated from byproducts; | A 21 % Chromat. B 35 % Chromat. |
2-(3-Iodo-propyl)-2-methyl-oxirane
A
1-methylcyclopentanol
B
(1-methylcyclobutyl)methanol
Conditions | Yield |
---|---|
With tert.-butyl lithium In diethyl ether; pentane at -78℃; Product distribution; Effect of additive or warming.; | |
With tert.-butyl lithium 1.) Et2O, pentane, -78 deg C, 5 min; 2.) warming; Yield given. Multistep reaction. Yields of byproduct given; |
1-iodo-5-hexanone
tert.-butyl lithium
A
2,2,3-trimethyl-3-heptanol
B
n-hexan-2-one
C
1-methylcyclopentanol
Conditions | Yield |
---|---|
In diethyl ether at -78℃; Title compound not separated from byproducts; | A 21 % Chromat. B 23 % Chromat. C 26 % Chromat. |
1-iodo-5-hexanone
A
2,2,3-trimethyl-3-heptanol
B
n-hexan-2-one
C
1-methylcyclopentanol
Conditions | Yield |
---|---|
With tert.-butyl lithium In diethyl ether at -78℃; Title compound not separated from byproducts; | A 21 % Chromat. B 23 % Chromat. C 26 % Chromat. |
With tert.-butyl lithium In diethyl ether at -78℃; Var.: n-BuLi, THF, -100 deg C; Title compound not separated from byproducts; | A 21 % Chromat. B 23 % Chromat. C 26 % Chromat. |
methylenecyclopentane
A
cyclopent-1-ene-1-methanol
B
1-Methylol-1-hydroxycyclopentan
C
2-methylenecyclopentan-1-ol
D
1-methylcyclopentanol
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride; oxygen 1) 60 grad C; Multistep reaction. Further byproducts given. Title compound not separated from byproducts; |
methyl-cyclopentane
A
2-Methylcyclopentanone
B
3-methyl-cyclopentanone
C
1-methylcyclopentanol
D
2-methylcyclopentanol
E
3-methylcyclopentanol
Conditions | Yield |
---|---|
With 2-Picolinic acid; water; Fe3O(OAc)6Pyr3.5 In pyridine; methanol at 25 - 30℃; Product distribution; 15-20 mA/cm2; in futher solvents; |
methyl-cyclopentane
A
2-Methylcyclopentanone
B
3-methyl-cyclopentanone
C
1-methylcyclopentanol
D
1-methylcyclopentyl acetate
Conditions | Yield |
---|---|
With N,N,N,N-tetraethylammonium tetrafluoroborate; (Fe3O(OAc)6)(C6H5N)3.5 In water; acetic acid; acetone Ambient temperature; 15-20 mA/cm2; Yield given. Further byproducts given. Yields of byproduct given; |
methyl-cyclopentane
A
2-Methylcyclopentanone
B
3-methyl-cyclopentanone
C
1-methylcyclopentanol
D
3-methylcyclopentanol
Conditions | Yield |
---|---|
With 2-Picolinic acid; (Fe3O(OAc)6)(C6H5N)3.5 In pyridine; water at 25 - 30℃; 15-20 mA/cm2; Yield given. Further byproducts given. Yields of byproduct given; |
Conditions | Yield |
---|---|
With water; hydrogen In gas Product distribution; Irradiation; gas-phase reaction of radiolytically formed cyclohexyl cation with water; evidence for cyclohexyl cation existence, structure and isomerisation of the C6H11+ ions; product yield dependence on pressure and composition of the gaseous system; | 100 % Chromat. |
With di(hydroxo)germanium (5,10,15,20-tetraphenylporphyrin) / silica gel composite In water Irradiation; Inert atmosphere; |
2-(3-Bromo-propyl)-2-methyl-oxirane
1-methylcyclopentanol
Conditions | Yield |
---|---|
With copper; triphenylphosphine In tetrahydrofuran | 95 % Chromat. |
With copper(l) iodide; lithium dihydronaphthylide radical; triphenylphosphine In tetrahydrofuran 1) -45 deg C, 5 min, -23 deg C, 3 h, r.t.; | 95 % Chromat. |
cyclohexyl cation
A
1-methylcyclopentanol
B
cyclohexanone
C
cyclohexanol
Conditions | Yield |
---|---|
With water In gas Product distribution; evidence for cyclohexyl cation existence, structure and isomerisation of the C6H11+ ions; product yield dependence on pressure and composition of the gaseous system; | A 23 % Chromat. B 23 % Chromat. C 54 % Chromat. |
dichloromethane
cyclopentanone
A
1-methylcyclopentanol
B
bicyclopentyl-1,1'-diol
Conditions | Yield |
---|---|
With water; lithium; 4,4'-di-tert-butylbiphenyl 1.) THF, -40 deg C, 55 min; Yield given. Multistep reaction. Yields of byproduct given; |
1-methylcyclopentyl acetate
1-methylcyclopentanol
Conditions | Yield |
---|---|
With perchloric acid In 1,4-dioxane at 15 - 45℃; Kinetics; |
4-oxo-nonanal
A
3-octanone
B
n-hexan-3-ol
C
n-hexan-2-ol
D
nonane-1,4-diol
E
n-hexan-2-one
F
1-methylcyclopentanol
Conditions | Yield |
---|---|
In hexane for 960h; Product distribution; Ambient temperature; thermal treatment; | A 8.17 % Chromat. B 0.74 % Chromat. C 0.95 % Chromat. D 5.25 % Chromat. E 1.56 % Chromat. F 0.78 % Chromat. |
1-methylcyclopentanol
6-chloro-2-hexanone
Conditions | Yield |
---|---|
With sodium hydrogencarbonate; iron(II) sulfate In tetrachloromethane Ambient temperature; in the dark; | 100% |
With lead(IV) acetate; lithium chloride at 20 - 35℃; for 4h; Oxidation; oxidative decyclization; mechanical activation; | 51% |
(i) aq. NaOCl, (ii) AgNO3, NaOH, aq. NH3; Multistep reaction; |
1-methylcyclopentanol
chloro-diphenylphosphine
(1-methylcyclopent-1-yloxy)di(phenyl)phosphine
Conditions | Yield |
---|---|
With dmap; triethylamine In tetrahydrofuran at 20℃; for 2h; | 98% |
With dmap; triethylamine In tetrahydrofuran at 20℃; for 2h; | 98% |
With dmap; triethylamine In tetrahydrofuran at 20℃; for 2h; | 95% |
1-methylcyclopentanol
6-Bromo-2-hexanone
Conditions | Yield |
---|---|
With bromine; potassium carbonate In chloroform at 0℃; for 5h; Bromination; retro-Barbier fragmentation; | 97% |
With [bis(acetoxy)iodo]benzene; sodium bromide In acetonitrile at 20℃; for 10h; Inert atmosphere; Irradiation; | 86% |
Stage #1: 1-methylcyclopentanol With potassium carbonate In chloroform at 0℃; for 0.25h; Stage #2: With bromine In chloroform at 0℃; for 2.5h; | 56% |
Conditions | Yield |
---|---|
95% | |
With iodine; oxalic acid | 87% |
With iodine Erhitzen des erhaltenen Gemisches von 1-Methyl-cyclopenten und Methylencyclopentan mit Essigsaeure und wenig Toluol-4-sulfonsaeure; |
Conditions | Yield |
---|---|
Stage #1: 1-methylcyclopentanol; sodium cyanide With sulfuric acid; acetic acid at 20℃; for 22.56h; Ritter Reaction; Stage #2: With sodium hydroxide; water at 0℃; pH=9; | 95% |
Conditions | Yield |
---|---|
With dmap; triethylamine In dichloromethane at 23℃; for 1h; Inert atmosphere; | 94% |
With dmap; triethylamine In tetrahydrofuran at 0 - 25℃; for 5h; Inert atmosphere; | 84% |
With dmap; triethylamine In tetrahydrofuran |
Conditions | Yield |
---|---|
Stage #1: 1-methylcyclopentanol With [bis(pyridine)iodine]+ tetrafluoroborate; caesium carbonate In dichloromethane at 20℃; for 8h; UV-irradiation; Stage #2: With sulfuric acid In water | 93% |
With [bis(pyridine)iodine]+ tetrafluoroborate; caesium carbonate In dichloromethane at 20℃; for 8h; Irradiation; | 93% |
With [bis(acetoxy)iodo]benzene; sodium iodide In acetonitrile at 20℃; for 10h; Inert atmosphere; Irradiation; | 78% |
With [bis(acetoxy)iodo]benzene; iodine In dichloromethane at 20℃; for 0.0833333h; UV-irradiation; |
t-butoxalyl chloride
1-methylcyclopentanol
Conditions | Yield |
---|---|
With pyridine; dmap In dichloromethane at 0 - 20℃; Inert atmosphere; | 93% |
Conditions | Yield |
---|---|
With cerium(III) chloride; tetrabutyl-ammonium chloride In acetonitrile for 12h; Inert atmosphere; Irradiation; | 84% |
Conditions | Yield |
---|---|
With bismuth(lll) trifluoromethanesulfonate; water Ritter reaction; | 82% |
With 1-methyl-3-(4-sulfonylbutyl)-1H-imidazol-3-ium trifluoromethanesulfonate; acetic acid at 80℃; for 24h; Ritter reaction; Inert atmosphere; Ionic liquid; | 65% |
1-methylcyclopentanol
4-methoxybenzonitrile
N-1-methylcyclopentane-4-methoxy-benzamide
Conditions | Yield |
---|---|
With 1-methyl-3-(4-sulfonylbutyl)-1H-imidazol-3-ium trifluoromethanesulfonate; acetic acid at 70℃; for 12h; Ritter reaction; Inert atmosphere; Ionic liquid; | 82% |
1-methylcyclopentanol
benzoyl triflate
1-methylcyclopentanol benzoate
Conditions | Yield |
---|---|
With pyridine In dichloromethane 1) 30 min, -78 deg C; 2) 1 h, room temperature; | 81% |
With pyridine In dichloromethane 1.) 0 deg C, 30 min, 2.) room temp., 1 h; | 81% |
1-methylcyclopentanol
propiononitrile
N-1-methylcyclopentane-propanamide
Conditions | Yield |
---|---|
With 1-methyl-3-(4-sulfonylbutyl)-1H-imidazol-3-ium trifluoromethanesulfonate; acetic acid at 65℃; for 24h; Ritter reaction; Inert atmosphere; Ionic liquid; | 81% |
Conditions | Yield |
---|---|
With caesium carbonate In acetonitrile at 20℃; for 24h; Inert atmosphere; | 80% |
2-furancarbonitrile
1-methylcyclopentanol
N-1-methylcyclopentane-furanamide
Conditions | Yield |
---|---|
With 1-methyl-3-(4-sulfonylbutyl)-1H-imidazol-3-ium trifluoromethanesulfonate; acetic acid at 80℃; for 12h; Ritter reaction; Inert atmosphere; Ionic liquid; | 78% |
Conditions | Yield |
---|---|
With cyclopentadienyl titanium(IV) trichloride; triethylsilyl chloride; zinc In tetrahydrofuran at 60℃; for 12h; Molecular sieve; Sealed tube; Inert atmosphere; | 77% |
Conditions | Yield |
---|---|
With lead(IV) acetate; ortho-chlorobenzoic acid at 20℃; for 20h; | 76% |
With lead(IV) acetate; ortho-chlorobenzoic acid for 20h; | 76% |
With lead(IV) acetate In acetic acid at 80℃; | 57 % Turnov. |
Conditions | Yield |
---|---|
With sulfuric acid; acetic acid at 0 - 20℃; for 3h; | 74% |
Conditions | Yield |
---|---|
With 1-methyl-3-(4-sulfonylbutyl)-1H-imidazol-3-ium trifluoromethanesulfonate; acetic acid at 40℃; for 24h; Ritter reaction; Inert atmosphere; Ionic liquid; | 73% |
With sulfuric acid |
1-methylcyclopentanol
acetic anhydride
A
1-methylcyclopentyl acetate
B
1'-methylcyclopentyl 3-oxobutanoate
C
dimethylglyoxal
Conditions | Yield |
---|---|
With cobalt(II) chloride In acetonitrile at 70℃; for 10h; | A 73% B 17% C n/a |
trimethylsilylazide
1-methylcyclopentanol
1-amino-1-methylcyclopentane hydrochloride
Conditions | Yield |
---|---|
Stage #1: trimethylsilylazide; 1-methylcyclopentanol With boron trifluoride diethyl etherate In benzene for 24h; Stage #2: With hydrogen; palladium 10% on activated carbon In methanol at 20℃; under 2327.23 Torr; for 1.5h; Stage #3: With hydrogenchloride In water | 71% |
Conditions | Yield |
---|---|
With C7H10N2*C8HF15O2 at 60℃; for 24h; neat (no solvent); | 70% |
With zinc(II) chloride |
Conditions | Yield |
---|---|
With pyridine; lead(IV) acetate; lithium chloride In benzene at 80℃; for 5h; | A 15% B 70% |
Conditions | Yield |
---|---|
With pyridine; lead(IV) acetate; sodium bromide In benzene at 80℃; for 3h; | A 15% B 70% |
With pyridine; lead(IV) acetate; lithium bromide In benzene at 80℃; for 3h; Product distribution; other MBr; | A n/a B 65 % Turnov. |
1-methylcyclopentanol
2,2,6-trimethyl-4H-1,3-dioxin-4-one
1'-methylcyclopentyl 3-oxobutanoate
Conditions | Yield |
---|---|
In xylene for 0.5h; Heating; | 70% |
Conditions | Yield |
---|---|
With lead(IV) acetate; ortho-chlorobenzoic acid for 20h; | 70% |
1-methylcyclopentanol
2-Methylpropionic anhydride
1-methylcyclopentyl isobutyrate
Conditions | Yield |
---|---|
With C7H10N2*C8HF15O2 at 60℃; for 24h; neat (no solvent); | 68% |
Conditions | Yield |
---|---|
In hexane at -40 - 20℃; for 3h; Inert atmosphere; Schlenk technique; | 68% |
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