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Phenyltrimethylammonium bromide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

16056-11-4

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Basic information
1. Product Name: Phenyltrimethylammonium bromide
2. Synonyms: TRIMETHYLPHENYLAMMONIUM BROMIDE;n,n,n-trimethylanilinium bromide;PHENYLTRIMETHYLAMMONIUM BROMIDE;n,n,n-trimethyl-benzenaminiubromide;n,n-trimethyl-benzenaminiumbromide;phenyltrimethyl-ammoniubromide;ro2-2979;N-Phenyl-N,N,N-trimethylammonium bromide
3. CAS NO:16056-11-4
4. Molecular Formula: Br*C₉H₁₄N
5. Molecular Weight: 216.12
6. EINECS: 240-202-8
7. Product Categories: Ammonium Bromides (Quaternary);Quaternary Ammonium Compounds
8. Mol File: 16056-11-4.mol
Chemical Properties
1. Melting Point: 215 °C (dec.)(lit.)
2. Boiling Point: N/A
3. Flash Point: N/A
4. Appearance: white to blue crystalline powder or chunks
5. Density: 1.2
6. Refractive Index: 1.5870 (estimate)
7. Storage Temp.: Refrigerator
8. Solubility: N/A
9. Water Solubility: almost transparency in Water
10. Sensitive: Hygroscopic
11. BRN: 3917006
12. CAS DataBase Reference: Phenyltrimethylammonium bromide(CAS DataBase Reference)
13. NIST Chemistry Reference: Phenyltrimethylammonium bromide(16056-11-4)
14. EPA Substance Registry System: Phenyltrimethylammonium bromide(16056-11-4)
Safety Data
1. Hazard Codes: Xi
2. Statements: 36/37/38
3. Safety Statements: 26-37/39
4. RIDADR: 2811
5. WGK Germany: 3
6. RTECS: BT2100000
7. TSCA: Yes
8. HazardClass: 6.1(b)
9. PackingGroup: III
10. Hazardous Substances Data: 16056-11-4(Hazardous Substances Data)

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16056-11-4 Usage

Chemical Properties

white to blue crystalline powder or chunks

Check Digit Verification of cas no

The CAS Registry Mumber 16056-11-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,0,5 and 6 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 16056-11:
(7*1)+(6*6)+(5*0)+(4*5)+(3*6)+(2*1)+(1*1)=84
84 % 10 = 4
So 16056-11-4 is a valid CAS Registry Number.

InChI:InChI=1/C9H14N.BrH/c1-10(2,3)9-7-5-4-6-8-9;/h4-8H,1-3H3;1H/q+1;/p-1

16056-11-4 Well-known Company Product Price

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(Code)Product description
CAS number
Packaging
Price
Detail

Aldrich
(135321) Trimethylphenylammoniumbromide 98%
16056-11-4
135321-100G
682.11CNY
Detail

16056-11-4Synthetic route

: 67-56-1
methanol

: 121-69-7
N,N-dimethyl-aniline

: 16056-11-4
N,N,N-trimethylanilinium bromide

Conditions	Yield
at 120 - 130℃; beim Erhitzen von feuchtem bromwasserstoffsauren Dimethylanilin im Druckrohr;

: 74-83-9
methyl bromide

: 121-69-7
N,N-dimethyl-aniline

: 16056-11-4
N,N,N-trimethylanilinium bromide

: 506-68-3
bromocyane

: 121-69-7
N,N-dimethyl-aniline

A: 18773-77-8
methyl(phenyl)cyanamide

B: 16056-11-4
N,N,N-trimethylanilinium bromide

: 506-96-7
Acetyl bromide

: 121-69-7
N,N-dimethyl-aniline

A: 579-10-2
N-acetyl-N-methylaniline

B: 16056-11-4
N,N,N-trimethylanilinium bromide

: 121-69-7
N,N-dimethyl-aniline

: 70-11-1
α-bromoacetophenone

A: 32119-53-2
N-methyl-N-phenacylaniline

B: 16056-11-4
N,N,N-trimethylanilinium bromide

: 121-69-7
N,N-dimethyl-aniline

: 107-82-4
i-pentyl bromide

A: 91935-09-0
N-isopentyl-N-methylaniline

B: 16056-11-4
N,N,N-trimethylanilinium bromide

Conditions	Yield
at 150 - 160℃;

: 121-69-7
N,N-dimethyl-aniline

: 535-11-5, 41978-69-2
Ethyl 2-bromopropionate

A: 214709-69-0
2-(methyl-phenyl-amino)-propionic acid ethyl ester

B: 16056-11-4
N,N,N-trimethylanilinium bromide

Conditions	Yield
at 125 - 130℃;

: 121-69-7
N,N-dimethyl-aniline

: 590-17-0
cyanomethyl bromide

: 16056-11-4
N,N,N-trimethylanilinium bromide

: 67-56-1
methanol

: 62-53-3
aniline

A: 16056-11-4
N,N,N-trimethylanilinium bromide

B: 121-69-7
N,N-dimethyl-aniline

Conditions	Yield
at 120 - 130℃; beim Erhitzen von bromwasserstoffsaurem Anilin;

: 4207-56-1
phenyltrimethylammonium tribromide

: 67-64-1
acetone

: 16056-11-4
N,N,N-trimethylanilinium bromide

Conditions	Yield
beim gelinden Erwaermen;

: 52045-06-4
tri-N-methyl-anilinium; dibromo iodate(I)

: 67-64-1
acetone

: 16056-11-4
N,N,N-trimethylanilinium bromide

: tri-N-methyl-anilinium; bromochloro iodate(I)

: 67-64-1
acetone

: 16056-11-4
N,N,N-trimethylanilinium bromide

: 121-69-7
N,N-dimethyl-aniline

: 572-09-8
2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl bromide

: 16056-11-4
N,N,N-trimethylanilinium bromide

Conditions	Yield
at 25℃;

: 32119-53-2
N-methyl-N-phenacylaniline

: 121-69-7
N,N-dimethyl-aniline

: 70-11-1
α-bromoacetophenone

A: 16056-11-4
N,N,N-trimethylanilinium bromide

B diphenylacyl-aniline: diphenylacyl-aniline

: 121-69-7
N,N-dimethyl-aniline

A: 16056-11-4
N,N,N-trimethylanilinium bromide

B hydrobromide of monomethylaniline: hydrobromide of monomethylaniline

Conditions	Yield
at 150℃; beim Erhitzen von bromwasserstoffsaurem Dimethylanilin;

: 121-69-7
N,N-dimethyl-aniline

: 70-11-1
α-bromoacetophenone

A: 16056-11-4
N,N,N-trimethylanilinium bromide

B N-methyl-N-phenacyl-aniline: N-methyl-N-phenacyl-aniline

: 121-69-7
N,N-dimethyl-aniline

: 70-11-1
α-bromoacetophenone

A: 41120-12-1
N,N-diphenacylaniline

B: 16056-11-4
N,N,N-trimethylanilinium bromide

C N-methyl-N-phenacyl-aniline: N-methyl-N-phenacyl-aniline

: 7732-18-5
water

: 4207-56-1
phenyltrimethylammonium tribromide

: 16056-11-4
N,N,N-trimethylanilinium bromide

Conditions	Yield
beim Kochen;

: 67-56-1
methanol

hydrobromide of dimethylaniline: hydrobromide of dimethylaniline

: 16056-11-4
N,N,N-trimethylanilinium bromide

: 121-69-7
N,N-dimethyl-aniline

: 70-11-1
α-bromoacetophenone

A: 16056-11-4
N,N,N-trimethylanilinium bromide

B methyl-phenacyl-aniline; diphenacyl-aniline: methyl-phenacyl-aniline; diphenacyl-aniline

: 16056-11-4
N,N,N-trimethylanilinium bromide

: 93296-10-7
(4-(dimethylamino)phenyl)zinc(II) chloride

: 1137-79-7
N,N-dimethyl-4-biphenylamine

Conditions	Yield
With C27H22Cl2N3NiP In tetrahydrofuran; 1-methyl-pyrrolidin-2-one for 12h; Inert atmosphere; Schlenk technique; Heating;	98%
With bis(tricyclohexylphosphine)nickel(II) dichloride In tetrahydrofuran; 1-methyl-pyrrolidin-2-one at 90℃; for 8h; Negishi coupling reaction; Inert atmosphere;	84%

: 16056-11-4
N,N,N-trimethylanilinium bromide

: 93296-09-4
4-methoxyphenylzinc chloride

: 613-37-6
4-methoxylbiphenyl

Conditions	Yield
With C27H22Cl2N3NiP In tetrahydrofuran; 1-methyl-pyrrolidin-2-one for 12h; Solvent; Inert atmosphere; Schlenk technique; Heating;	98%
With C38H34Br2N4Ni2P2 In tetrahydrofuran; 1-methyl-pyrrolidin-2-one at 65℃; for 12h; Inert atmosphere; Schlenk technique;	94%
With C32H26ClN2NiP In tetrahydrofuran; 1-methyl-pyrrolidin-2-one at 85℃; for 12h; Inert atmosphere;	74%

: 16056-11-4
N,N,N-trimethylanilinium bromide

: 90252-89-4
p-tolylzinc(II) chloride

: 644-08-6
4-Methylbiphenyl

Conditions	Yield
With C27H22Cl2N3NiP In tetrahydrofuran; 1-methyl-pyrrolidin-2-one for 12h; Inert atmosphere; Heating; Schlenk technique;	90%

: 1182669-71-1
N-(2-methylbenzoyl)-8-aminoquinoline

: 16056-11-4
N,N,N-trimethylanilinium bromide

: 1609401-42-4
2,6-dimethyl-N-(quinolin-8-yl)benzamide

Conditions	Yield
With nickel(II) triflate; sodium carbonate; triphenylphosphine In toluene at 160℃; for 14h;	90%

: 16056-11-4
N,N,N-trimethylanilinium bromide

: 2C9H14N(1+)*Br6Te2(2-)

Conditions	Yield
With tellurium; bromine In acetonitrile for 24h; Heating;	88%

: 16056-11-4
N,N,N-trimethylanilinium bromide

: phenyltrimethylammonium hexabromoselenate

Conditions	Yield
With selenium; bromine In acetonitrile Heating;	87%

: 16056-11-4
N,N,N-trimethylanilinium bromide

: phenyltrimetylammonium selenocyanate

: phenyltrimethylammonium hexabromoselenate

Conditions	Yield
With bromine In acetonitrile Ambient temperature;	86%

: 16056-11-4
N,N,N-trimethylanilinium bromide

: 73183-34-3
bis(pinacol)diborane

: 13327-62-3
2-mercaptopyridine sodium salt

A: 18438-38-5
2-methylsulfanyl-pyridine

B: 24388-23-6
2-phenyl-4,4,5,5-tetramethyl-1,3,2-dioxoborole

C: 121-69-7
N,N-dimethyl-aniline

D: 108-95-2
phenol

Conditions	Yield
In acetonitrile at 30 - 35℃; for 24h; Irradiation; Inert atmosphere;	A 64% B 22% C 81% D 6%

: 16056-11-4
N,N,N-trimethylanilinium bromide

: 73183-34-3
bis(pinacol)diborane

: 24388-23-6
2-phenyl-4,4,5,5-tetramethyl-1,3,2-dioxoborole

Conditions	Yield
With 10H-phenothiazine; caesium carbonate In acetonitrile for 18h; Irradiation; Sealed tube; Inert atmosphere;	76%

: 16056-11-4
N,N,N-trimethylanilinium bromide

: 766-97-2
4-n-methylphenylacetylene

: 3287-02-3
4-(phenylethynyl)toluene

Conditions	Yield
With SIPr-PdCl2-Py; sodium t-butanolate In tetrahydrofuran at 45℃; for 4h; Sonogashira Cross-Coupling; Inert atmosphere;	60%

: disodium closo-dodecaborate

: 1643-19-2
tetrabutylammomium bromide

: 16056-11-4
N,N,N-trimethylanilinium bromide

: 122-04-3
4-nitro-benzoyl chloride

A: [N(C4H9)4]2 (hydroxo)undecahydro-closo-dodecaborane

B: 2(CH3)3(C6H5)N(1+)*B12H11COC6H4NO2(2-) = [(CH3)3(C6H5)N]2(B12H11COC6H4NO2)

Conditions	Yield
In acetone byproducts: NaCl; stirring (-20°C, 30 min and 20°C, 20 h); pptn., drying; elem. anal.;	A 1% B 58%

: 16056-11-4
N,N,N-trimethylanilinium bromide

: 13327-62-3
2-mercaptopyridine sodium salt

A: 18438-38-5
2-methylsulfanyl-pyridine

B: 3111-54-4
2-phenylsulfanylpyridine

C: 121-69-7
N,N-dimethyl-aniline

D: 108-95-2
phenol

Conditions	Yield
In acetonitrile at 30 - 35℃; for 24h; Irradiation; Inert atmosphere;	A 49% B 22% C 37% D 15%

: 16056-11-4
N,N,N-trimethylanilinium bromide

: 84109-17-1
2-methylphenylzinc chloride

: 643-58-3
2-methylbiphenyl

Conditions	Yield
With C27H22Cl2N3NiP In tetrahydrofuran; 1-methyl-pyrrolidin-2-one for 12h; Inert atmosphere; Heating; Schlenk technique;	46%

: 439145-80-9
5-Acetyl-2-benzyloxy-N-[3,5-bis(trifluoromethyl)phenyl]benzamide

: 16056-11-4
N,N,N-trimethylanilinium bromide

: 439145-82-1
2-Benzyloxy-5-(2-bromoacetyl)-N-[3,5-bis(trifluoromethyl)phenyl]benzamide

Conditions	Yield
In tetrahydrofuran	42.7%

: 16056-11-4
N,N,N-trimethylanilinium bromide

: 6427-70-9
benzyltrimethylammonium hexafluorophosphate

Conditions	Yield
With ammonium hexafluorophosphate In water; acetone for 4h; Inert atmosphere; Schlenk technique;	40%

: 16056-11-4
N,N,N-trimethylanilinium bromide

: 13139-86-1
4-methoxyphenyl magnesium bromide

: 613-37-6
4-methoxylbiphenyl

Conditions	Yield
With 1,3-bis[(diphenylphosphino)propane]dichloronickel(II) In tetrahydrofuran at 20℃; for 48h; Inert atmosphere;	12%

: 16056-11-4
N,N,N-trimethylanilinium bromide

: 3,4-dibromo-tri-N-methyl-anilinium; bromide

Conditions	Yield
With bromine; iron at 100 - 120℃;

: 16056-11-4
N,N,N-trimethylanilinium bromide

: tri-N-methyl-anilinium; bromide, compound with bromine

Conditions	Yield
With bromine; acetic acid

: 16056-11-4
N,N,N-trimethylanilinium bromide

: 3-bromo-tri-N-methyl-anilinium; bromide

Conditions	Yield
With bromine; iron at 70℃;

: 16056-11-4
N,N,N-trimethylanilinium bromide

: 4207-56-1
phenyltrimethylammonium tribromide

Conditions	Yield
With bromine

: 16056-11-4
N,N,N-trimethylanilinium bromide

: 52045-06-4
tri-N-methyl-anilinium; dibromo iodate(I)

Conditions	Yield
With iodine(I) bromide; acetic acid

: 16056-11-4
N,N,N-trimethylanilinium bromide

: phenyltrimethylammonium dichloroiodate

Conditions	Yield
With Iodine monochloride; acetic acid
With iodine trichloride; acetic acid

: 16056-11-4
N,N,N-trimethylanilinium bromide

: tri-N-methyl-anilinium; bromochloro iodate(I)

Conditions	Yield
With Iodine monochloride; acetic acid

: 16056-11-4
N,N,N-trimethylanilinium bromide

: 16091-28-4
tri-N-methyl-anilinium; dichloro bromate(I)

Conditions	Yield
With chlorine; acetic acid at 60℃;

: 16056-11-4
N,N,N-trimethylanilinium bromide

: tri-N-methyl-anilinium; bromide, compound with iodine

Conditions	Yield
With iodine; acetic acid at 100℃;

: 16056-11-4
N,N,N-trimethylanilinium bromide

A: 74-83-9
methyl bromide

B: 121-69-7
N,N-dimethyl-aniline

Conditions	Yield
at 240℃;
In dimethylsulfoxide-d6 at 120℃; for 0.333333h;

16056-11-4Upstream product

16056-11-4Downstream Products

16056-11-4Relevant academic research and scientific papers

7-SUBSTITUTED BENZOFURAN DERIVATIVES

-

, (2008/06/13)

The present disclosure is concerned with new benzofuran derivatives and a process for the preparation thereof. The present benzofuran derivatives are useful as β-adrenergic blocking agents.

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