5-METHOXYGRAMINE

Product Name: 5-METHOXYGRAMINE
CAS No.: 16620-52-3
Chemical Name: 5-METHOXYGRAMINE
Synonyms: NSC 88885;methoxygramine;5-METHOXYGRAMINE;TIMTEC-BB SBB003509;5-METHOXYGRAMINE 99%;5-Methoxygramine,99%;3-ETHYL-1H-PYRAZOL-5-AMINE HCL;2-dimethylaminomethyl-5-methoxyindole;5-methoxy-3-(dimethylaminomethyl)indole;3-(DIMETHYLAMINOMETHYL)-5-METHOXY-INDOLE
CBNumber: CB5245525
Molecular Formula: C12H16N2O
Formula Weight: 204.27
MOL File: 16620-52-3.mol

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5-METHOXYGRAMINE Property

Melting point:: 123-126 °C (lit.)
Boiling point:: 342.77°C (rough estimate)
Density: 1.0565 (rough estimate)
refractive index: 1.6000 (estimate)
storage temp.: Refrigerator (+4°C)
pka: 16.70±0.30(Predicted)
BRN: 170533
CAS DataBase Reference: 16620-52-3(CAS DataBase Reference)

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Safety

Hazard Codes: C,Xi
Risk Statements: 34-22
Safety Statements: 22-24/25
WGK Germany: 3
RTECS: NL7700000
F: 10
HS Code: 29339900
Toxicity: mouse,LD50,intraperitoneal,130mg/kg (130mg/kg),Psychopharmacologia Vol. 16, Pg. 385, 1970.

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Hazard and Precautionary Statements (GHS)

Symbol(GHS)

Signal word

Danger

Hazard statements

H302Harmful if swallowed

H314Causes severe skin burns and eye damage

Precautionary statements

P260Do not breathe dust/fume/gas/mist/vapours/spray.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P270Do not eat, drink or smoke when using this product.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.

P301+P330+P331IF SWALLOWED: Rinse mouth. Do NOT induce vomiting.

P303+P361+P353IF ON SKIN (or hair): Remove/Take off Immediately all contaminated clothing. Rinse SKIN with water/shower.

P304+P340IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P310Immediately call a POISON CENTER or doctor/physician.

P321Specific treatment (see … on this label).

P330Rinse mouth.

P363Wash contaminated clothing before reuse.

P405Store locked up.

P501Dispose of contents/container to..…

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N-Bromosuccinimide Price

Sigma-Aldrich

Product number: M14870
Product name: 5-Methoxygramine
Purity: 99%
Packaging: 5g
Price: $225
Updated: 2023/06/20

TRC

Product number: M263278
Product name: 5-Methoxygramine
Packaging: 10mg
Price: $45
Updated: 2021/12/16

AK Scientific

Product number: Y7751
Product name: N-[(5-Methoxy-1H-indol-3-yl)methyl]-N,N-dimethylamine
Packaging: 1g
Price: $104
Updated: 2021/12/16

American Custom Chemicals Corporation

Product number: CHM0031161
Product name: 5-METHOXYGRAMINE
Purity: 95.00%
Packaging: 1G
Price: $654.89
Updated: 2021/12/16

American Custom Chemicals Corporation

Product number: CHM0031161
Product name: 5-METHOXYGRAMINE
Purity: 95.00%
Packaging: 5G
Price: $970.2
Updated: 2021/12/16

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5-METHOXYGRAMINE Chemical Properties,Usage,Production

Chemical Properties

white to almost white crystalline powder

Uses

• ;Reactant for preparation of dopamine D2 receptor antagonists1• ;Reactant for asymmetric preparation of ethenyl(tetrahydro)carbazoledicarboxylates via gold(I)-catalyzed intramolecular Friedel-Crafts allylic alkylation reaction2• ;Reactant for preparation of N-substituted 3-aryl-8-azabicyclo[3.2.1]octan-3-ols as dopamine D2-like receptor ligands3• ;Reactant for preparation of substituted N-trimethoxybenzoyl indoles, indolines, and a tetrahydroquinoline via N-aroylation with trimethoxybenzoyl chloride or anhydride as antitubulin agents4• ;Reactant for preparation of in

Uses

Reactant for preparation of dopamine D2 receptor antagonists
Reactant for asymmetric preparation of ethenyl(tetrahydro)carbazoledicarboxylates via gold(I)-catalyzed intramolecular Friedel-Crafts allylic alkylation reaction
Reactant for preparation of N-substituted 3-aryl-8-azabicyclo[3.2.1]octan-3-ols as dopamine D2-like receptor ligands
Reactant for preparation of substituted N-trimethoxybenzoyl indoles, indolines, and a tetrahydroquinoline via N-aroylation with trimethoxybenzoyl chloride or anhydride as antitubulin agents
Reactant for preparation of indolylmethanesulfonamide and its methoxy derivatives

5-METHOXYGRAMINE Preparation Products And Raw materials

Raw materials

5-Methoxyindole Formaldehyde Diethyl ether Hydrochloric acid Acetic acid Sodium hydroxide Dimethylamine

Preparation Products

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5-METHOXYGRAMINE Suppliers

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16620-52-3, 5-METHOXYGRAMINERelated Search:

Gramine 4-Methoxygramine 6-METHOXYGRAMINE 5-BENZYLOXYGRAMINE 3-DIMETHYLAMINOMETHYL-5-METHOXY-1H-INDOLE-2-CARBOXYLIC ACID ETHYL ESTER 2-ACETYL-8-TRIFLUOROMETHOXY-2,3,4,5-TETRAHYDRO-1H-PYRIDO[4,3-B]INDOLE (5-METHOXY-1H-INDOL-3-YL)(PIPERIDINO)METHANETHIONE Oxybis((5,3-indolylene)methylene)bis(trimethylammonium) bis(methyl sul fate) 5-METHOXY-2-METHYLGRAMINE 5-ETHYL-2-(5-METHOXY-1H-INDOL-3-YL)-7-METHYL-1,3-DIAZATRICYCLO[3.3.1.1~3,7~]DECAN-6-ONE 5-METHOXYGRAMINE 8-BENZYLOXY-2-METHYL-2,3,4,5-TETRAHYDRO-1H-PYRIDO[4,3-B]INDOLE AKOS JY2083007 2-ACETYL-8-METHOXY-2,3,4,5-TETRAHYDRO-1H-PYRIDO[4,3-B]INDOLE 1-[(5-methoxy-1H-indol-3-yl)methyl]-2-oxo-1,2-dihydropyridine-3-carboxylic acid AKOS JY2083279

5-METHOXYGRAMINE 99%

5-Methoxygramine, N,N-Dimethyl-(5-methoxy-1H-indol-3-yl)methylamine

methoxygramine

5-Methoxygramine or 5-Methoxy-3-(Dimethylaminomethyl)-indole

(5-methoxy-1H-indol-3-yl)methyl-dimethylammonium

3-ETHYL-1H-PYRAZOL-5-AMINE HCL

5-Methoxygramine,99%

NSC 88885

3-((dimethylamino)methyl)-5-methoxy-indol

5-methoxy-3-(dimethylaminomethyl)indole

5-methoxy-n,n-dimethyl-1h-indole-3-methanamin

TIMTEC-BB SBB003509

3-[(Dimethylamino)methyl]-5-methoxy-1H-indole

3-(DIMETHYLAMINOMETHYL)-5-METHOXY-INDOLE

(5-METHOXY-1H-INDOL-3-YLMETHYL)-DIMETHYL-AMINE

5-METHOXYGRAMINE

2-dimethylaminomethyl-5-methoxyindole

N-[(5-METHOXY-1H-INDOL-3-YL)METHYL]-N,N-DIMETHYLAMINE

1H-Indole-3-methanamine, 5-methoxy-N,N-dimethyl-

16620-52-3

Heterocyclic Building Blocks

Indoles

Building Blocks

C12

Chemical Synthesis

Heterocyclic Building Blocks

Indoles

Indoline & Oxindole

Heterocyclic Compounds

Indoles and derivatives