Rastim 30 dkv

Base Information

Chemical Name:Rastim 30 dkv
CAS No.:119584-53-1
Molecular Formula:C₁₆H₁₃NO₃S
Molecular Weight:299.35
Hs Code.:
DSSTox Substance ID:DTXSID00923008
Nikkaji Number:J2.117.938H
Mol file:119584-53-1.mol

Synonyms:3-(benzyloxycarbonylmethyl)-2-benzothiazolinone;Rastim 30 DKV

Suppliers and Price of Rastim 30 dkv

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

American Custom Chemicals Corporation
3-(BENZYLOXYCARBONYLMETHYL)BENZOTHIAZOLINONE 95.00%
5MG
$ 505.58

Total 1 raw suppliers

Chemical Property of Rastim 30 dkv

Chemical Property:

Vapor Pressure:3.97E-09mmHg at 25°C
Boiling Point:473.3°Cat760mmHg
Flash Point:240.1°C
PSA：76.54000
Density:1.337g/cm³
LogP:2.80640
XLogP3:3.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:5
Exact Mass:299.06161445
Heavy Atom Count:21
Complexity:395

Purity/Quality:: 3-(BENZYLOXYCARBONYLMETHYL)BENZOTHIAZOLINONE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)COC(=O)CN2C3=CC=CC=C3SC2=O

Technology Process of Rastim 30 dkv

There total 4 articles about Rastim 30 dkv 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: 72.0%

: 881-10-7
2-oxo-3-benzothiazolineacetyl chloride

: 100-51-6,185532-71-2
benzyl alcohol

: 119584-53-1
3-(benzyloxycarbonylmethyl)-benzothiazoline

Guidance literature:: With triethylamine; In tetrahydrofuran; for 24h; Heating;

Reference yield:

: 934-34-9
2(3H)-Benzothiazolone

: 119584-53-1
3-(benzyloxycarbonylmethyl)-benzothiazoline

Guidance literature:: Multi-step reaction with 3 steps

1: 80 percent / 25percent aq. NaOH, K₂CO₃ / 1.)90-100 deg C, 6 h 2.)25-30 deg C, 18 h

2: 72 percent / SOCl₂ / benzene / 3 h / Heating

3: 72 percent / Et₃N / tetrahydrofuran / 24 h / Heating

With sodium hydroxide; thionyl chloride; potassium carbonate; triethylamine; In tetrahydrofuran; benzene;

Reference yield:

: 945-03-9
(2-oxo-1,3-benzothiazol-3(2H)-yl)acetic acid

: 119584-53-1
3-(benzyloxycarbonylmethyl)-benzothiazoline

Guidance literature:: Multi-step reaction with 2 steps

1: 72 percent / SOCl₂ / benzene / 3 h / Heating

2: 72 percent / Et₃N / tetrahydrofuran / 24 h / Heating

With thionyl chloride; triethylamine; In tetrahydrofuran; benzene;