4-tert-Butyl-benzamidine

Base Information

Chemical Name:4-tert-Butyl-benzamidine
CAS No.:125772-42-1
Molecular Formula:C11H16N2
Molecular Weight:176.26
Hs Code.:2925290090
DSSTox Substance ID:DTXSID00401038
Nikkaji Number:J1.949.269I
Mol file:125772-42-1.mol

Synonyms:4-tert-Butyl-benzamidine;125772-42-1;4-(tert-Butyl)benzimidamide;4-tert-butylbenzenecarboximidamide;4-tert-butylbenzamidine;4-tert-butylbenzimidamide;SCHEMBL421322;DTXSID00401038;NFNSHLXROFMSCN-UHFFFAOYSA-N;MFCD05662846;4-tert-butylbenzene-1-carboximidamide;AKOS009312074;SB32293;FT-0755263;EN300-1865891

Suppliers and Price of 4-tert-Butyl-benzamidine

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

Matrix Scientific
4-(tert-Butyl)benzimidamide 95%
10g
$ 1480.00

Matrix Scientific
4-(tert-Butyl)benzimidamide 95%
25g
$ 2220.00

Labseeker
4-Tert-Butyl-Benzamidine 95
10g
$ 2163.00

American Custom Chemicals Corporation
4-TERT-BUTYL-BENZAMIDINE 95.00%
1G
$ 909.56

Alichem
4-(tert-Butyl)benzimidamide
1g
$ 180.18

AK Scientific
4-Tert-butyl-benzamidine
25g
$ 3047.00

Total 12 raw suppliers

Chemical Property of 4-tert-Butyl-benzamidine

Chemical Property:

Vapor Pressure:0.0121mmHg at 25°C
Boiling Point:260.6°C at 760 mmHg
Flash Point:111.4°C
PSA：49.87000
Density:0.99g/cm³
LogP:3.06820
XLogP3:2.6
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:176.131348519
Heavy Atom Count:13
Complexity:183

Purity/Quality:

97% ^*data from raw suppliers

4-(tert-Butyl)benzimidamide 95% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)(C)C1=CC=C(C=C1)C(=N)N

Technology Process of 4-tert-Butyl-benzamidine

There total 1 articles about 4-tert-Butyl-benzamidine 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: 74.5%

: 4210-32-6
4-tert-butyl benzonitrile

: 125772-42-1
4-(tert-butyl)benzimidamide

Guidance literature:: 4-tert-butyl benzonitrile; With lithium hexamethyldisilazane; In tetrahydrofuran; at 0 - 20 ℃; for 16h;

With hydrogenchloride; In tetrahydrofuran; water; at 0 ℃;