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5-METHOXY-4-METHYLINDOLE

5-METHOXY-4-METHYLINDOLE structure

CAS No.: 302912-21-6

Chemical Name:: 5-METHOXY-4-METHYLINDOLE

Synonyms: 4-Methyl-5-methoxyindole;5-METHOXY-4-METHYLINDOLE;5-Methoxy-4-Methyl-1H-indole;5-Methoxy-4-Methylindole 98%;1H-Indole, 5-Methoxy-4-Methyl-

CBNumber:: CB0354121

Molecular Formula:: C10H11NO

Molecular Weight:: 161.2

MDL Number:: MFCD01863615

MOL File:: 302912-21-6.mol

MSDS File:: SDS

Last updated:2023-07-12 17:02:35

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5-METHOXY-4-METHYLINDOLE Properties

Melting point	76-79 °C (lit.)
Boiling point	303.3±22.0 °C(Predicted)
Density	1.134±0.06 g/cm3(Predicted)
storage temp.	2-8°C
pka	17.06±0.30(Predicted)

SAFETY

Risk and Safety Statements

Symbol(GHS)	GHS07
Signal word	Warning
Hazard statements	H315-H319-H335
Precautionary statements	P261-P305+P351+P338
Hazard Codes	Xi
Risk Statements	36/37/38
Safety Statements	26-36
WGK Germany	3

5-METHOXY-4-METHYLINDOLE price More Price(8)

Manufacturer	Product number	Product description	CAS number	Packaging	Price	Updated	Buy
American Custom Chemicals Corporation	CHM0012756	5-METHOXY-4-METHYLINDOLE 95.00%	302912-21-6	1G	$769.49	2021-12-16	Buy
Matrix Scientific	144929	5-Methoxy-4-methyl-1H-indole 95%	302912-21-6	5g	$1101	2021-12-16	Buy
Matrix Scientific	144929	5-Methoxy-4-methyl-1H-indole 95%	302912-21-6	25g	$3633	2021-12-16	Buy
aablocks	AA002ZFR	5-Methoxy-4-methyl-1h-indole 95%	302912-21-6	100mg	$88	2021-12-16	Buy
aablocks	AA002ZFR	5-Methoxy-4-methyl-1h-indole 95%	302912-21-6	250mg	$133	2021-12-16	Buy

Product number	Packaging	Price	Buy
CHM0012756	1G	$769.49	Buy
144929	5g	$1101	Buy
144929	25g	$3633	Buy
AA002ZFR	100mg	$88	Buy
AA002ZFR	250mg	$133	Buy

5-METHOXY-4-METHYLINDOLE Chemical Properties,Uses,Production

Uses

Reactant for preparation of β-carboline-1-carboxylic acids as inhibitors of mitogen activated protein kinase-activated protein kinase 2. Reactant for preparation of indolyl and isoquinolinyl anthranilates as PPARδ partial agonists 2

Uses

Reactant for preparation of β-carboline-1-carboxylic acids as inhibitors of mitogen activated protein kinase-activated protein kinase 2
Reactant for preparation of indolyl and isoquinolinyl anthranilates as PPARδ partial agonists

General Description

5-Methoxy-4-methylindole or 5-methoxy-4-methyl-1H-indole is a substituted 1H-indole. Its efficacy as a substrate for indigoid production has been evaluated.

5-METHOXY-4-METHYLINDOLE Preparation Products And Raw materials

Raw materials

Preparation Products

5-METHOXY-4-METHYLINDOLE Suppliers

Global( 42)Suppliers

Supplier	Tel	Email	Country	ProdList	Advantage
CONIER CHEM AND PHARMA LIMITED	+8618523575427	sales@conier.com	China	47465	58
KARMEL TECHNOLOGY (HK) CO.,LIMITED	+8618795957998	karmelhk@126.com	CHINA	2886	58
Henan Alfa Chemical Co., Ltd	+8618339805032	alfa4@alfachem.cn	China	12755	58
LEAPCHEM CO., LTD.	+86-852-30606658	market18@leapchem.com	China	43348	58
Amadis Chemical Company Limited	571-89925085	sales@amadischem.com	China	131981	58
Tetranov Biopharm	13526569071	sales@leadmedpharm.com	China	7891	64
The future of Shanghai Industrial Co., Ltd.	021-61552785	sales@shshiji.com	China	9552	55
ShangHai AmK Pharmaceutical Technology Co., Ltd.	18019252918	sale@amkchem.com	China	15415	55
Sigma-Aldrich	021-61415566 800-8193336	orderCN@merckgroup.com	China	51471	80
Codow Chemical Co.,Ltd.	18620099427	amy@howeipharm.com	China	17698	55

Supplier	Advantage
CONIER CHEM AND PHARMA LIMITED	58
KARMEL TECHNOLOGY (HK) CO.,LIMITED	58
Henan Alfa Chemical Co., Ltd	58
LEAPCHEM CO., LTD.	58
Amadis Chemical Company Limited	58
Tetranov Biopharm	64
The future of Shanghai Industrial Co., Ltd.	55
ShangHai AmK Pharmaceutical Technology Co., Ltd.	55
Sigma-Aldrich	80
Codow Chemical Co.,Ltd.	55

5-METHOXY-4-METHYLINDOLE Spectrum

5-METHOXY-4-METHYLINDOLE(302912-21-6)IR

302912-21-6(5-METHOXY-4-METHYLINDOLE)Related Search:

5-METHOXY-4-METHYLINDOLE Indometacin 1-[P-CHLOROBENZOYL]-5-METHOXY-2-METHYLINDOLE-3-ACETIC ACID CARBOXYMETHYL ESTER 5-METHOXY-2-METHYLINDOLE,5-Methoxy-2-methylindole, 99+% 4-METHOXY-1-METHYLINDOLE

3-Formyl-5-methoxy-1-methylindole,5-METHOXY-1-METHYLINDOLE-3-CARBOXALDEHYDE 5-METHOXY-2-METHYLINDOLE-3-ACETIC ACID 4-Methylindole 5-Methoxy-4-methylindole-3-carboxaldehyde 3,6A,11,14-TETRAHYDRO-9-METHOXY-2-METHYL-(12H)-ISOQUINO[1,2-B]PYRROLO[3,2-F][1,3]BENZOXAZINE-1-CARBOXYLIC ACID, ETHYL ESTER

N-(2-PHENYLETHYL)-1-P-CHLOROBENZOYL-5-METHOXY-2-METHYLINDOLE-3-ACETAMIDE N-(4-ACETAMIDOPHENYL)-1-P-CHLOROBENZOYL-5-METHOXY-2-METHYLINDOLE-3-ACETAMIDE N-(3-PYRIDYL)-1-P-CHLOROBENZOYL-5-METHOXY-2-METHYLINDOLE-3-ACETAMIDE 1-(4-CHLOROBENZYL)-5-METHOXY-2-METHYLINDOLE-3-ACETIC ACID 5-METHOXY-7-METHYLINDOLE-2-CARBOXYLIC ACID ETHYL ESTER

6-METHOXY-7-METHYLINDOLE 5-METHOXY-7-METHYLINDOLE-2-CARBOXYLIC ACID 4-METHOXY-7-METHYLINDOLE

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5-METHOXY-4-METHYLINDOLE 5-Methoxy-4-Methylindole 98% 4-Methyl-5-methoxyindole 5-Methoxy-4-Methyl-1H-indole 1H-Indole, 5-Methoxy-4-Methyl- 302912-21-6 Indoles Heterocyclic Building Blocks Building Blocks Building Blocks Heterocyclic Building Blocks Indoles Heterocyclic Compounds