Benzamide, N-(bis(1-aziridinyl)phosphinyl)-p-chloro-

Base Information

Chemical Name:Benzamide, N-(bis(1-aziridinyl)phosphinyl)-p-chloro-
CAS No.:27807-69-8
Molecular Formula:C₁₁H₁₃ClN₃O₂P
Molecular Weight:285.67
Hs Code.:
DSSTox Substance ID:DTXSID90182127
Nikkaji Number:J68.063J
Wikidata:Q83052788
Mol file:27807-69-8.mol

Synonyms:Benzamide, N-(bis(1-aziridinyl)phosphinyl)-p-chloro-;n-[bis(aziridin-1-yl)phosphoryl]-4-chlorobenzamide;BRN 0258690;27807-69-8;A-20;AI3-62257;N-(Bis(1-aziridinyl)phosphinyl)-p-chlorobenzamide;Benzamide, N-(bis(1-aziridinyl)phosphinyl)-4-chloro-;C11H13ClN3O2P;DTXSID90182127;C11-H13-Cl-N3-O2-P;LS-25771

Suppliers and Price of Benzamide, N-(bis(1-aziridinyl)phosphinyl)-p-chloro-

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

Sigma-Aldrich
Anti-TNAP3 antibody produced in rabbit affinity isolated antibody
100 μg
$ 410.00

Total 12 raw suppliers

Chemical Property of Benzamide, N-(bis(1-aziridinyl)phosphinyl)-p-chloro-

Chemical Property:

PSA：62.00000
Density:1.5g/cm³
LogP:2.07580
Storage Temp.:-20°C
XLogP3:1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:285.0433914
Heavy Atom Count:18
Complexity:374

Purity/Quality:

99% ^*data from raw suppliers

Anti-TNAP3 antibody produced in rabbit affinity isolated antibody ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CN1P(=O)(NC(=O)C2=CC=C(C=C2)Cl)N3CC3

Technology Process of Benzamide, N-(bis(1-aziridinyl)phosphinyl)-p-chloro-

There total 2 articles about Benzamide, N-(bis(1-aziridinyl)phosphinyl)-p-chloro- 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:

: 619-56-7
4-chlorobenzamide

: 27807-69-8
N-(bis-aziridin-1-yl-phosphinoyl)-4-chloro-benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: H₂O; PCl₅

2: benzene; triethylamine

With phosphorus pentachloride; water; triethylamine; benzene;