CAS No.127-25-3,METHYL ABIETATE Suppliers,MSDS download

Dayang Chem (Hangzhou) Co.,Ltd.

DayangChem exported this product to many countries and regions at best price. If you are looking for the material's manufacturer or supplier in China, DayangChem is your best choice. Pls contact with us freely for getting detailed product spe

1-Phenanthrenecarboxylicacid, 1,2,3,4,4a,4b,5,6,10,10a-decahydro-1,4a-dimethyl-7-(1-methylethyl)-,methyl ester, (1R,4aR,4bR,10aR)-

Cas:127-25-3

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Ality Chemical Corporation

The 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 providi

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Shanghai Upbio Tech Co.,Ltd

1.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

1-Phenanthrenecarboxylicacid, 1,2,3,4,4a,4b,5,6,10,10a-decahydro-1,4a-dimethyl-7-(1-methylethyl)-,methyl ester, (1R,4aR,4bR,10aR)-

Cas:127-25-3

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Henan Wentao Chemical Product Co., Ltd.

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

1-Phenanthrenecarboxylicacid, 1,2,3,4,4a,4b,5,6,10,10a-decahydro-1,4a-dimethyl-7-(1-methylethyl)-,methyl ester, (1R,4aR,4bR,10aR)-

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Hangzhou Keyingchem Co.,Ltd

Hangzhou 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

METHYL ABIETATE

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Zibo Hangyu Biotechnology Development Co., Ltd

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

1-Phenanthrenecarboxylicacid, 1,2,3,4,4a,4b,5,6,10,10a-decahydro-1,4a-dimethyl-7-(1-methylethyl)-,methyl ester, (1R,4aR,4bR,10aR)-

Cas:127-25-3

Min.Order:10 Gram

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Henan Tianfu Chemical Co., Ltd.

Product Name: METHYL ABIETATE Synonyms: ABALYN;METHYL ABIETATE;METHYL ESTER OF ROSIN;1,2,3,4,4a,4b,5,6,10,10a-decahydro-1,4a-dimethyl-7-(1-methylethyl)-,methylester,[1R-(1.alpha.,1-Phenanthrenecarboxylicacid;13-dien-15-oicacid,13-isopropyl-podocar

127-25-3

Cas:127-25-3

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Xi`an Eastling Biotech Co., Ltd.

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

METHYL ABIETATE

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Antimex Chemical Limied

factory?direct?sale Application:healing drugs

1-Phenanthrenecarboxylicacid, 1,2,3,4,4a,4b,5,6,10,10a-decahydro-1,4a-dimethyl-7-(1-methylethyl)-,methyl ester, (1R,4aR,4bR,10aR)-

Cas:127-25-3

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Hangzhou Fandachem Co.,Ltd

1-Phenanthrenecarboxylicacid, 1,2,3,4,4a,4b,5,6,10,10a-decahydro-1,4a-dimethyl-7-(1-methylethyl)-,methyl ester, (1R,4aR,4bR,10aR)- cas 127-25-3Appearance:white crystalline powder Storage:Store in dry, dark and ventilated place Package:25KG drum Appl

1-Phenanthrenecarboxylicacid, 1,2,3,4,4a,4b,5,6,10,10a-decahydro-1,4a-dimethyl-7-(1-methylethyl)-,methyl ester, (1R,4aR,4bR,10aR)- cas 127-25-3

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Hebei Quanhe Biotechnology Co. LTD

1. Timely and efficient service to ensure communication with customers2. Produce products of different specifications and sizes according to your requirements.3. Quality procedures and standards recognized by SGS. Advanced plant equipment ensures sta

METHYL ABIETATE

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Changzhou Extraordinary Pharmatech co.,LTD

Changzhou Extraordinary Pharmatech co., LTD. As a leading chemical manufacturer and supplier in China.DAS authentication is passed.We can provide the popular precursor chemicals, we have our own strong R & D team, have our own laboratories and fa

Methyl Abietate

Cas:127-25-3

Min.Order:1 Gram

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Hebei youze Biotechnology Co.,Ltd

1: Fast and guaranteed shipment (TNT;EMS;FEDEX;DHL;UPS;EUB, special line) 2: Various payment terms accepted (Btc;MoneyGram;WU) 3: Valued package (Paraffin coating; Double aluminum foil bag; Vacuum packaging) 4: Efficient delivery (3-10 DAYS fast deli

methyl abietate CAS:127-25-3 the cheapest price

Cas:127-25-3

Min.Order:1 Kilogram

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Shanghai Run-Biotech Co., Ltd.

Shanghai, Run-Biotech Co., Ltd is a leading domestic pharmaceutical, biopharmaceutical, and health care products R & D outsourcing services company. As an innovation-driven and customer-focused company, Run Biotech provides a broad and integrated por

METHYL ABIETATE

Cas:127-25-3

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Skyrun Industrial Co.,Ltd

Price, Purity Application:reagent

CSR081605-62358

Cas:127-25-3

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Synthetic route

: 186581-53-3, 908094-01-9
diazomethane

: 514-10-3
abietic acid

: 127-25-3
methyl abietate

Conditions

Conditions	Yield
In diethyl ether at 0℃;	100%
In diethyl ether at 0℃; for 0.166667h;	99%
With diethyl ether

: 514-10-3
abietic acid

: 77-78-1
dimethyl sulfate

: 127-25-3
methyl abietate

Conditions

Conditions	Yield
With lithium hydroxide In N,N-dimethyl-formamide	100%
With lithium hydroxide In N,N-dimethyl-formamide	100%
With potassium carbonate In acetone at 20℃;	100%

: 514-10-3
abietic acid

: 616-38-6
carbonic acid dimethyl ester

: 127-25-3
methyl abietate

Conditions

Conditions	Yield
With lithium hydroxide monohydrate In N,N-dimethyl-formamide at 93 - 100℃; Reagent/catalyst; Concentration; Inert atmosphere;	99.6%

: 514-10-3
abietic acid

: 74-88-4
methyl iodide

: 127-25-3
methyl abietate

Conditions

Conditions	Yield
With potassium carbonate In acetone for 14h; Reflux;	99%
With potassium carbonate In acetone for 12h; Reflux;	93%
With potassium carbonate In N,N-dimethyl-formamide at 20℃; for 24h;	81%

: 514-10-3
abietic acid

: 18107-18-1
diazomethyl-trimethyl-silane

: 127-25-3
methyl abietate

Conditions

Conditions	Yield
In methanol; diethyl ether; toluene at 20℃; for 0.5h;	94%

: 67-71-0
dimethylsulfone

: 514-10-3
abietic acid

: 127-25-3
methyl abietate

Conditions

Conditions	Yield
With lithium hydroxide In N,N-dimethyl-formamide at 20℃; for 16h;	86%

: 67-56-1
methanol

: 514-10-3
abietic acid

: 127-25-3
methyl abietate

Conditions

Conditions	Yield
Stage #1: abietic acid With 1H-imidazole; iodine; triphenylphosphine In dichloromethane at 20℃; for 0.0833333h; Garegg-Samuelsson type reaction; Stage #2: methanol In dichloromethane at 20℃; Garegg-Samuelsson type reaction;	84%
With sulfuric acid for 36h; Heating;	45%
at 260 - 285℃; under 56634.1 - 88260.9 Torr;
With sulfuric acid

: 67-56-1
methanol

: 19897-44-0
7,13-Abietadien-18-oic acid anhydride

: 127-25-3
methyl abietate

Conditions

Conditions	Yield
With sulfuric acid In benzene at 65℃; for 30h; Esterification;	49%

: 67-56-1
methanol

A: 127-25-3
methyl abietate

B: 25236-84-4
<1R-(1α,4aβ,4bα,6α,10aα)>-1,2,3,4,4a,4b,5,6,10,10a-decahydro-1,4a-dimethyl-6-methoxy-7-(1-methylethyl)-phenanthrenecarboxylic acid methylester

C: <1R-(1α,4aβ,4bα,6β,10aα)>-1,2,3,4,4a,5,6,10,10a-decahydro-1,4a-dimethyl-6-methoxy-7-(1-methylethyl)-phenanthrenecarboxylic acid methylester

Conditions

Conditions	Yield
With iodine; copper dichloride; iron tricarbonyl 1) dibutylether, 3 d, heating, 2) diethylether, 2 h, r.t.; Yield given. Multistep reaction. Yields of byproduct given;	A 1.5% B n/a C n/a
With iodine; copper dichloride; iron tricarbonyl 1) dibutylether, 3 days, heating, 2) diethylether, 2 h, r.t.; Yield given. Multistep reaction. Yields of byproduct given;	A 1.5% B n/a C n/a

...Expand

: 77-78-1
dimethyl sulfate

potassium-salt of/the/ abietic acid: potassium-salt of/the/ abietic acid

: 127-25-3
methyl abietate

: 14351-66-7
abietic acid sodium salt

: 127-25-3
methyl abietate

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: diethyl ether / 11 h / 25 °C 2: 49 percent / H2SO4 / benzene / 30 h / 65 °C View Scheme
Multi-step reaction with 2 steps 1: diethyl ether / 3 h / 20 °C 2: 49 percent / H2SO4 / benzene / 30 h / 65 °C View Scheme

: 127-25-3
methyl abietate

: 666-84-2
abietinol

Conditions

Conditions	Yield
With sodium bis(2-methoxyethoxy)aluminium dihydride In toluene for 6.5h; Ambient temperature;	100%
With lithium aluminium tetrahydride In diethyl ether at 0℃; for 1h;	99%
With lithium aluminium tetrahydride In diethyl ether for 0.666667h; Reduction; Heating;	98%

: 127-25-3
methyl abietate

: 228863-80-7
methyl <1aR(1aβ,2aα,3α,6aβ,7α,7aβ)>-decahydro-7a-peroxyformtacetal-7-<(4-methyl-3-oxoketal)pentyl>-3,6a-dimethylnaphth<2,3-b>oxiran-3-carboxylate

Conditions

Conditions	Yield
With pyridine; oxygen; ozone In dichloromethane at -70℃;	92%
With ozone In dichloromethane at -78℃;	78%

: 108-31-6
maleic anhydride

: 127-25-3
methyl abietate

: 54868-63-2
maleopimaric acid methyl ester

Conditions

Conditions	Yield
Stage #1: methyl abietate at 180℃; for 3h; Inert atmosphere; Stage #2: maleic anhydride With toluene-4-sulfonic acid; acetic acid for 12h; Diels-Alder reaction; Reflux;	90%
With zeolite NIC-2β In toluene for 7h; Heating;	0.04 g
With zeolite NIC-2β In toluene for 7h; Product distribution; Heating; also with α-methylacrolein or acrolein; var. catalysts, solvents;	0.04 g

: 127-25-3
methyl abietate

: 1235-74-1, 1757-97-7, 2756-34-5, 7151-00-0, 10178-27-5, 10178-29-7, 21699-55-8, 24035-60-7
Methyl dehydroabietate

Conditions

Conditions	Yield
With 5% Pd(II)/C(eggshell) at 240 - 250℃; Neat (no solvent);	85%
With palladium on activated charcoal at 240℃; Inert atmosphere;	85%
With aluminum oxide; palladium/alumina at 230℃;
With magnesium hydrosilicate; palladium at 230℃;
With palladium on activated charcoal at 240℃; for 3h;

: 127-25-3
methyl abietate

: 22552-63-2
methyl 13β,14β-dihydroxyabieta-7-en-18-oate

Conditions

Conditions	Yield
With pyridine; potassium osmate(VI) dihydrate; water; 4-methylmorpholine N-oxide In acetone for 168h; Reflux; regioselective reaction;	85%
With pyridine; osmium(VIII) oxide; trimethylamine-N-oxide In tert-butyl alcohol for 168h; Inert atmosphere; Reflux; regioselective reaction;	70%
With pyridine; osmium(VIII) oxide; trimethylamine-N-oxide In water; tert-butyl alcohol for 24h; Product distribution; Heating; var. ratios of the educt;	68%
With pyridine; osmium(VIII) oxide; trimethylamine-N-oxide In water; tert-butyl alcohol for 24h; Heating;	68%

: 127-25-3
methyl abietate

: 514-10-3
abietic acid

Conditions

Conditions	Yield
With Me2AlTeMe In toluene at 23℃; for 8h;	85%

: 127-25-3
methyl abietate

: 369387-06-4
methyl 7-hydroxy-13-isopropylpodocarpe-8,11,13-trien-15-oate

Conditions

Conditions	Yield
With tert.-butylhydroperoxide; selenium(IV) oxide In octane; dichloromethane for 12h;	83%

: 127-25-3
methyl abietate

: 228863-82-9
methyl <1aR(1aβ,2aα,3α,6aβ,7α,7aβ)>-decahydro-7a-formyl-7-(4-methyl-3-oxopentyl)-3,6a-dimethylnaphth<2,3-b>oxiran-3-carboxylate

Conditions

Conditions	Yield
With pyridine; oxygen; ozone In methanol at -70℃;	79%
Multi-step reaction with 2 steps 1: 78 percent / ozone / CH2Cl2 / -78 °C 2: 80 percent / triphenylphosphine / CH2Cl2 / 12 h / Ambient temperature View Scheme

: 127-25-3
methyl abietate

: 108-24-7
acetic anhydride

: 22565-68-0
methyl (1R,4aS,9R,10aR)-9-acetoxy-1,2,3,4,4a,9,10,10a-octahydro-1,4a-dimethyl-7-(1-methylethyl)phenanthrene-1-carboxylate

Conditions

Conditions	Yield
With selenium(IV) oxide for 3h; Ambient temperature;	68%

: 127-25-3
methyl abietate

: 762-42-5
dimethyl acetylenedicarboxylate

: (Z)-2-((1R,4aS,9R,10aR)-7-Isopropyl-1-methoxycarbonyl-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydro-phenanthren-9-yl)-but-2-enedioic acid dimethyl ester

Conditions

Conditions	Yield
at 210℃; under 60004.8 - 86256.9 Torr; for 25h;	60%

: 127-25-3
methyl abietate

: 92215-39-9
methyl 7-oxoabiet-13(14)-ene-18-oate

Conditions

Conditions	Yield
With water; iodine; potassium hydrogencarbonate In diethyl ether at 20℃; for 24h; Inert atmosphere;	60%

: 127-25-3
methyl abietate

: 19402-34-7
methyl abieta-8,13(15)-dien-18-oate

Conditions

Conditions	Yield
Stage #1: methyl abietate With hydrogen bromide In acetic acid for 20h; Stage #2: With lithium hydroxide In N,N-dimethyl-formamide at 80℃; for 16h; Heating;	56%
Multi-step reaction with 2 steps 1: 47 percent / 33percent HBr / acetic acid / 6 h / Ambient temperature 2: 71 percent / lithium hydroxide monohydrate / dimethylformamide / 3.5 h / 80 °C View Scheme
Multi-step reaction with 2 steps 1: 35 percent / 37percent HBr / acetic acid / 6.5 h / Ambient temperature 2: 74 percent / LiOH*H2O / dimethylformamide / 3.5 h / 80 °C View Scheme

: 127-25-3
methyl abietate

A: 13082-81-0
9-hydroxy-13-isopropyl-podocarpadien-(7.13)-oic acid-(15)-methyl ester

B: 17751-34-7
7,8-Dihydro-7β-hydroxy-8,9,10,11-dehydroabietinsaeure-methylester

Conditions

Conditions	Yield
With selenium(IV) oxide In acetonitrile for 24h;	A 48% B 32%

: 127-25-3
methyl abietate

A: 1802-09-1
methyl 7-hydroxy-13-isopropylpodocarpe-8,11,13-trien-15-oate

B: 17751-34-7
7,8-Dihydro-7β-hydroxy-8,9,10,11-dehydroabietinsaeure-methylester

Conditions

Conditions	Yield
With selenium(IV) oxide In acetonitrile for 24h;	A 48% B 32%

: 127-25-3
methyl abietate

A: 92215-39-9
[1R,(1α,4αβ,4βα,8αβ,10αα)]-1,2,3,4,4a,4b,5,6,8a,9,10,10a-dodecahydro-1,4a-dimethyl-7-(1-methylethyl)-9-oxo-1-phenanthrenecarboxylic acid methyl ester

B: 55177-17-8
(1aS,3aR,4R,7aR,7bR,9aS)-9a-Isopropyl-4,7a-dimethyl-1a,3,3a,4,5,6,7,7a,7b,8,9,9a-dodecahydro-1-oxa-cyclopropa[a]phenanthrene-4-carboxylic acid methyl ester

Conditions

Conditions	Yield
With iodine; potassium hydrogencarbonate In diethyl ether; water at 30℃; for 3h;	A 48% B n/a

: 127-25-3
methyl abietate

: 22628-83-7
methyl 8,15-dibromoabietan-18-oate

Conditions

Conditions	Yield
With hydrogen bromide In acetic acid for 6h; Ambient temperature;	47%
With hydrogen bromide In acetic acid for 6.5h; Ambient temperature;	35%

: 127-25-3
methyl abietate

: 925-90-6
ethylmagnesium bromide

: C22H34O

Conditions

Conditions	Yield
With titanium(IV) isopropylate In tetrahydrofuran; diethyl ether at 0 - 20℃; for 4h; Inert atmosphere;	47%

: 127-25-3
methyl abietate

: 546-67-8
lead(IV) tetraacetate

A: 1235-74-1, 1757-97-7, 2756-34-5, 7151-00-0, 10178-27-5, 10178-29-7, 21699-55-8, 24035-60-7
Methyl dehydroabietate

B: 22565-68-0
methyl (1R,4aS,9R,10aR)-9-acetoxy-1,2,3,4,4a,9,10,10a-octahydro-1,4a-dimethyl-7-(1-methylethyl)phenanthrene-1-carboxylate

C: 127488-29-3
(1R,4aS,4bS,10aR)-4b-Acetoxy-7-isopropyl-1,4a-dimethyl-1,2,3,4,4a,4b,5,6,10,10a-decahydro-phenanthrene-1-carboxylic acid methyl ester

Conditions

Conditions	Yield
In acetic acid at 80℃; for 7h;	A 37% B 43% C 17%

...Expand

: 127-25-3
methyl abietate

: 920-37-6
2-Chloroacrylonitrile

: 155507-60-1
Methyl 17,19-dinoratis-14-chloro-14-cyano-15-ene-16-(1-methylethyl)-4-carboxylate

Conditions

Conditions	Yield
With 10H-phenothiazine at 170℃; for 15h;	39%

: 127-25-3
methyl abietate

: 69226-51-3
2,2,2-trichloroethyl sulfamate

: methyl 7-(((2,2,2-trichloroethoxy)sulfonyl)amino)-8,11,13-abietatrien-18-oate

Conditions

Conditions	Yield
With bis{rhodium[3,3'-(1,3-phenylene)bis(2,2-dimethylpropanoic acid)]}; bis(tertbutylcarbonyloxy)iodobenzene In benzene at 23℃; stereoselective reaction;	36%

: 127-25-3
methyl abietate

A: 18178-76-2
methyl 7β,14β-dihydroxy-13-isopropyl-8-podocarpan-15α-oate

B: 18125-91-2
methyl 7β-Hydroxy-13α-isopropylpodocarp-8(14)-en-15α-oate

C: methyl 7β-Hydroxy-13-isopropyl-8β-podocarp-13(14)-en-15α-oate

D: methyl 14β-Hydroxy-13α-isopropylpodocarp-7(8)-en-15α-oate

Conditions

Conditions	Yield
Stage #1: methyl abietate With sodium tetrahydroborate; boron trifluoride diethyl etherate In tetrahydrofuran at 20℃; for 3.5h; Inert atmosphere; Stage #2: With dihydrogen peroxide; sodium acetate In tetrahydrofuran; water for 16h; Inert atmosphere;	A 26% B 22% C 10% D 34%

...Expand

: 127-25-3
methyl abietate

A: 1235-74-1, 1757-97-7, 2756-34-5, 7151-00-0, 10178-27-5, 10178-29-7, 21699-55-8, 24035-60-7
Methyl dehydroabietate

B: 13082-81-0
9-hydroxy-13-isopropyl-podocarpadien-(7.13)-oic acid-(15)-methyl ester

C: 1802-09-1
methyl 7-hydroxy-13-isopropylpodocarpe-8,11,13-trien-15-oate

D: 17751-34-7
7,8-Dihydro-7β-hydroxy-8,9,10,11-dehydroabietinsaeure-methylester

Conditions

Conditions	Yield
With selenium(IV) oxide In carbon disulfide for 24h; Ambient temperature;	A 16% B 30% C 10% D 9%
With selenium(IV) oxide In 1,4-dioxane for 24h; Product distribution; Ambient temperature; various solvents (C6H6, CS2, Et2O, MeCN, t-BuOH, Ac2O); oxidation with lead tetraacetate;	A 17% B 29% C 17% D 18%

...Expand

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