Uses
ChemicalBook > CAS DataBase List > 1,3,5-TRIBENZYLHEXAHYDRO-1,3,5-TRIAZINE

1,3,5-TRIBENZYLHEXAHYDRO-1,3,5-TRIAZINE

Uses
Product Name
1,3,5-TRIBENZYLHEXAHYDRO-1,3,5-TRIAZINE
CAS No.
2547-66-2
Chemical Name
1,3,5-TRIBENZYLHEXAHYDRO-1,3,5-TRIAZINE
Synonyms
LABOTEST-BB LT00138201;1,3,5-Tribenzyl-1,3,5-triazinane;1,3,5-TRIBENZYLHEXAHYDRO-S-TRIAZINE;1,3,5-TRIBENZYLHEXAHYDRO-1,3,5-TRIAZINE;Hexahydro-1,3,5-tribenzyl-1,3,5-triazine;1,3,5-Tribenzylhexahydro-1,3,5-triazine 98%;1,3,5-TRIBENZYLHEXAHYDRO-1,3,5-TRIAZINE 98+%;Hexahydro-1,3,5-tris(phenylmethyl)-1,3,5-triazine;1,3,5-Triazine, hexahydro-1,3,5-tris(phenylmethyl)-;1,3,5-Tribenzylhexahydro-1,3,5-triazine, 98+% white powder
CBNumber
CB3431861
Molecular Formula
C24H27N3
Formula Weight
357.49
MOL File
2547-66-2.mol
More
Less

1,3,5-TRIBENZYLHEXAHYDRO-1,3,5-TRIAZINE Property

Melting point:
49-51 °C(lit.)
Boiling point:
100 °C0.005 mm Hg(lit.)
Density 
113
refractive index 
1.6270 (estimate)
Flash point:
>230 °F
storage temp. 
Sealed in dry,Room Temperature
pka
5.46±0.20(Predicted)
InChIKey
VWVZIRPJPFJGFE-UHFFFAOYSA-N
More
Less

Safety

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-37/39
WGK Germany 
3
HS Code 
29336990
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P271Use only outdoors or in a well-ventilated area.

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

P302+P352IF ON SKIN: wash with plenty of soap and water.

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

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
337722
Product name
1,3,5-Tribenzylhexahydro-1,3,5-triazine
Purity
98%
Packaging
25g
Price
$173
Updated
2023/06/20
Alfa Aesar
Product number
H25964
Product name
1,3,5-Tribenzylhexahydro-1,3,5-triazine, 98+%
Packaging
5g
Price
$49.65
Updated
2024/03/01
Alfa Aesar
Product number
H25964
Product name
1,3,5-Tribenzylhexahydro-1,3,5-triazine, 98+%
Packaging
25g
Price
$156.65
Updated
2024/03/01
TRC
Product number
T768950
Product name
1,3,5-Tribenzylhexahydro-1,3,5-triazine
Packaging
10g
Price
$105
Updated
2021/12/16
Matrix Scientific
Product number
099576
Product name
1,3,5-Tribenzyl-1,3,5-triazinane
Purity
95+%
Packaging
10g
Price
$119
Updated
2021/12/16
More
Less

1,3,5-TRIBENZYLHEXAHYDRO-1,3,5-TRIAZINE Chemical Properties,Usage,Production

Uses

1,3,5-Tribenzyl-1,3,5-triazinane is used as a reagent in the synthesis of phosphinic acid based N-Acetylated alpha-linked acidic dipeptidase (NAALADase) inhibitors, which may potentially be used for the treatment of both neurodegenerative disorders and peripheral neuropathies.

Uses

1,3,5-Tribenzylhexahydro-1,3,5-triazine is used as a reagent in the synthesis of phosphinic acid based NAALADase inhibitors which may potentially be used for the treatment of both neurodegenerative disorders and peripheral neuropathies.

Uses

1,3,5-Tribenzylhexahydro-1,3,5-triazine was used:

  • in the synthesis of alkyl β-aminocarboxylates via trifluoromethanesulfonic acid catalyzed reaction with ketene silyl acetals
  • as ligand to study the assembling process of a heterogeneous Cr-based single-site ethylene trimerization catalyst by X-ray absorption spectroscopy
  • as ligand during conversion of Phillips Cr/SiO2 polymerisation catalyst to ethylene trimerisation catalyst after assembling new active sites on the silica surface

Application

1,3,5-Tribenzylhexahydro-1,3,5-triazine was used:in the synthesis of alkyl β-aminocarboxylates via trifluoromethanesulfonic acid catalyzed reaction with ketene silyl acetals;as ligand to study the assembling process of a heterogeneous Cr-based single-site ethylene trimerization catalyst by X-ray absorption spectroscopy;as ligand during conversion of Phillips Cr/SiO2 polymerisation catalyst to ethylene trimerisation catalyst after assembling new active sites on the silica surface.

Synthesis


To a round-bottomed flask (125 mL) equipped with a reflux condenser was added theappropriate amine (0.05 mmol), toluene (40 mL) and formaldehyde (37%, 4.1 mL).The solution was brought to reflux using an external oil bath and kept stirring for 30min. Then, the toluene was evaporated under reduced pressure, and the residue wasdissolved in ethyl acetate and washed with a saturated aqueous solution of sodiumchloride. After evaporation of the solvent under reduced pressure in a rotaryevaporator, the residue was purified by silica gel column chromatography usinghexane/ethyl acetate 9:1 as the eluent.

1,3,5-TRIBENZYLHEXAHYDRO-1,3,5-TRIAZINE Preparation Products And Raw materials

Raw materials

Preparation Products

More
Less

1,3,5-TRIBENZYLHEXAHYDRO-1,3,5-TRIAZINE Suppliers

Toronto Research Chemicals Inc.
Tel
--
Fax
--
Email
info@trc-canada.com
Country
Canada
ProdList
6668
Advantage
58
More
Less

View Lastest Price from 1,3,5-TRIBENZYLHEXAHYDRO-1,3,5-TRIAZINE manufacturers

Career Henan Chemical Co
Product
1,3,5-TRIBENZYLHEXAHYDRO-1,3,5-TRIAZINE 2547-66-2
Price
US $500.00/KG
Min. Order
1KG
Purity
98%
Supply Ability
1ton
Release date
2018-08-04

2547-66-2, 1,3,5-TRIBENZYLHEXAHYDRO-1,3,5-TRIAZINERelated Search:


  • 1,3,5-Triazine, hexahydro-1,3,5-tris(phenylmethyl)-
  • 1,3,5-TRIBENZYLHEXAHYDRO-1,3,5-TRIAZINE 98+%
  • Hexahydro-1,3,5-tribenzyl-1,3,5-triazine
  • Hexahydro-1,3,5-tris(phenylmethyl)-1,3,5-triazine
  • 1,3,5-Tribenzyl-1,3,5-triazinane
  • 1,3,5-TRIBENZYLHEXAHYDRO-1,3,5-TRIAZINE
  • 1,3,5-TRIBENZYLHEXAHYDRO-S-TRIAZINE
  • LABOTEST-BB LT00138201
  • 1,3,5-Tribenzylhexahydro-1,3,5-triazine 98%
  • 1,3,5-Tribenzylhexahydro-1,3,5-triazine, 98+% white powder
  • 2547-66-2
  • C24H27N3
  • Heterocyclic Building Blocks
  • Triazines
  • Building Blocks
  • Building Blocks
  • Heterocyclic Building Blocks
  • Triazines
  • Heterocyclic Building Blocks
  • Heterocyclic Compounds