Basic Information | Post buying leads | Suppliers | Cas Database |
Name |
4-Methylbenzene-1-carboximidamide hydrochloride |
EINECS | N/A |
CAS No. | 6326-27-8 | Density | N/A |
PSA | 49.87000 | LogP | 2.88110 |
Solubility | N/A | Melting Point |
211-214 ºC |
Formula | C8H10N2.HCl | Boiling Point | 225°C at 760 mmHg |
Molecular Weight | 170.642 | Flash Point | 89.9°C |
Transport Information | N/A | Appearance | N/A |
Safety | 26-36/37/39-37/39 | Risk Codes | R36/37/38 |
Molecular Structure | Hazard Symbols | ||
Synonyms |
Benzenecarboximidamide,4-methyl-, monohydrochloride (9CI);p-Toluamidine, monohydrochloride (8CI);4-Methylbenzamidinehydrochloride;4-Toluamidine hydrochloride;p-Methylbenzamidine hydrochloride; |
Article Data | 8 |
The 4-Methylbenzene-1-carboximidamide hydrochloride with cas registry number of 6326-27-8, its other registry number is 39800-79-8. Its systematic name is benzenecarboximidamide, 4-methyl-, monohydrochloride (9ci). The 4-Methylbenzene-1-carboximidamide hydrochloride belongs to the following product categories: (1)blocks; (2)BuildingBlocks; (3)Carboxes; (4)Miscellaneous.
Preparation: this chemical can be prepared by 4-methyl-benzonitrile with reaction temperature of 25 ℃. This reaction will need reagent sodium methoxide, NH4Cl and solvent methanol. The yield is about 30%.
Uses of 4-Methylbenzene-1-carboximidamide hydrochloride: it can be used to produce 3-bromo-3-p-tolyl-3H-diazirine with reaction time of 1 hours. This reaction will need reagent NaOBr, LiBr and solvent dimethylsulfoxide.
When you are using this chemical, please be cautious about it as the following:
The 4-Methylbenzene-1-carboximidamide hydrochloride irritates to eyes, respiratory system and skin. When use it, wear suitable protective clothing, gloves and eye/face protection. If contact with eyes, rinse immediately with plenty of water and seek medical advice.
You can still convert the following datas into molecular structure:
(1)InChI: InChI=1/C8H10N2.ClH/c1-6-2-4-7(5-3-6)8(9)10;/h2-5H,1H3,(H3,9,10);1H;
(2)Smiles: C(c1ccc(cc1)C)(=N)N.Cl.