O-CHLORAMINE T

Base Information

Chemical Name:O-CHLORAMINE T
CAS No.:110076-44-3
Molecular Formula:C7H7ClNNaO2S
Molecular Weight:227.647
Hs Code.:
Mol file:110076-44-3.mol

Synonyms:O-TOLUENESULFONCHLORAMIDE SODIUM SALT;O-CHLORAMINE T;SODIUM O-TOLUENESULFONCHLORAMIDE;Chloramine;O-CHLORAMINE T2-HYDRATE;O-CHLORAMINE T DIHYDRATE;Sodium o-Toluenesulfonchloramide o-Toluenesulfonchloramide Sodium Salt;o-ChloraMine T

Suppliers and Price of O-CHLORAMINE T

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

TRC
o-ChloramineT
250mg
$ 45.00

Biosynth Carbosynth
o-Chloramine T
500 g
$ 452.00

Biosynth Carbosynth
o-Chloramine T
250 g
$ 266.00

Biosynth Carbosynth
o-Chloramine T
100 g
$ 133.00

Biosynth Carbosynth
o-Chloramine T
50 g
$ 78.00

Biosynth Carbosynth
o-Chloramine T
25 g
$ 46.00

American Custom Chemicals Corporation
O-CHLORAMINE T 95.00%
500G
$ 14400.00

American Custom Chemicals Corporation
O-CHLORAMINE T 95.00%
25G
$ 1100.00

AK Scientific
o-ChloramineTdihydrate
25g
$ 112.00

Total 9 raw suppliers

Chemical Property of O-CHLORAMINE T

Chemical Property:

PSA：60.98000
LogP:3.16340
Solubility.:Aqueous Acid (Slightly), Aqueous Base (Slightly)

Purity/Quality:

98%,99%, ^*data from raw suppliers

o-ChloramineT ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:
Statements: 22-31-34-42
Safety Statements: 7-22-26-36/37/39

MSDS Files:: SDS file from LookChem

Useful:

Uses o-Chloramine T is a useful reagent for the preparation of 1-bromoalkyne and 1-iodoalkyne compounds.

Technology Process of O-CHLORAMINE T

There total 1 articles about O-CHLORAMINE T which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 88-19-7
methyl 2-(aminosulfonyl)benzoate

: 507-40-4
tert-butylhypochlorite

: 110076-44-3
N-chloro-toluene-2-sulfonamide; sodium-salt

Guidance literature:: With sodium hydroxide; tert-butyl alcohol;
DOI:10.1021/ja01643a082

Reference yield: 90.0%

: 6303-88-4
9-methyl-2,3,4,9-tetrahydro-1H-carbazole

: 110076-44-3
N-chloro-toluene-2-sulfonamide; sodium-salt

: 2-methyl-N-(9-methyl-2,3,4,9-tetrahydro-1H-carbazol-1-yl)benzenesulfonamide

Guidance literature:: With iodine; In 1,4-dioxane; at 20 ℃; for 9h; regioselective reaction; Green chemistry;
DOI:10.1021/acs.joc.8b00286

Reference yield:

: 24393-52-0
ethyl (E)-3-(4-chlorophenyl)prop-2-enoate

: 110076-44-3
N-chloro-toluene-2-sulfonamide; sodium-salt

: (2R,3S)-3-(4-Chloro-phenyl)-2-hydroxy-3-(toluene-2-sulfonylamino)-propionic acid ethyl ester

Guidance literature:: With potassium osmate(VI); Hydroquinone 1,4-phthalazinediyl diether; In water; acetonitrile; at 20 ℃;
DOI:10.1002/anie.200501180