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Sr. Structure of the Product and Name
of C. A. S. No.M.
Uses And Type
Of No the
Structure
Reaction Involved . |
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| p- Chloro Benzoic
Acid |
|
[74-11-3] |
M. P. |
Oxidation Reaction |
 |
98%
Purity [PCBA] Mol. F. C7
H5ClO2 Mol. Wt.
156.566
|
|
|
239-241°C
|
Intermediate For The Synthesis Of The Drug
Mebendazole. |
2. 3-Nitro-4- ChloroBenzoic
Acid M.
P.
For the synthesis
of
Mebendazole |
|
 |
98% Purity [NCBA] Mol F. C7 H4
Cl N O4 Mol. Wt.
201.564 |
|
180-182°C
|
A
Product of the unit operation Nitration |
| 3. 4-Amino-3-Nitro Benzoic Acid |
|
 |
98% Purity [NABA] Mol. F.
C7 H6 N2 O4 Mol. Wt.
182.134
|
[1588-83-6] |
290
°C |
In the synthesis of
Dyes and Dyes stuff intermediates
The Nucleophillic
Aromatic Substitution Reaction Amination
|
4.
3-Nitro-4-Chlorobenzophenone
98-102°C For
the
synthesisof
Mebendazole. |
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 |
98% Purity
[NCBP] Mol. F. C13 H8 Cl N
O3
Mol. Wt. 261.660
|
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It’s a
Friedel-Crafts Reaction
Aroylation
|
5 4-
amino-3-Nitrbenzophenone
116-120°C
In the synthesis
of
Mebendzole |
|
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>98% Purity [NABP] Mol. F. C13
H10 N2 O3 Mol. Wt
242.230
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| 6 4-
Amino-3-Nitrbenzophenone
[616-79-5] 278
°C |
|
 |
> 98% Purity [NABA]
Mol. F. C7 H6 N2
O4
Mol. Wt. 182.134 |
|
|
For the dyes and
dyestuff intermediates
The Nucleophillic
Aromatic Substitution Reaction Amination
|
| 7 3,4-Diaminobenzophenone
116-120°C |
|
 |
[DABP]
>98% Purity Mol. F. C13 H12
N2 O
Mol. Wt 212.247
|
|
|
For the synthesis of
Mebendazole
The Reduction of
–NO2 gr. to –NH2 gr.
|
| 8 4-Chlorobenzophenone |
|
 |
[PCBP]
>98% Purity
Mol. F. C13
H9 Cl O
Mol. Wt
216.663
|
[134-85-0] |
M. P.
76
B. P.
195 - 196 at 17 mm
Hg
|
For The Synthesis Of
The Drug Citrazene
|
| 9 b-Phethyl
Mthyl Ether
[PME]
[3558-60-9] |
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 |
> 98%
Purity
Mol. F. C9 H12 O
Mol. Wt. 136.191
|
|
B. P.
80 °C/20
mm
|
The Intermediate for
the Synthesis of Methoxy Ethyl Phenol
The Alkohol
Etherification
|
| 10 b-[4’-Nitro Phethyl] Mthyl
Ether |
|
 |
> 98%
Purity Mol. F. C9 H11
N O3
Mol. Wt. 181.189
|
M. P.
65-70°C
|
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The Intermediate for
the Synthesis of Methoxy Ethyl Phenol
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