GB330862A - Improvements in or relating to the manufacture of 3.3-dichloro-4.4-dihydroxy-5.5-diacetylamino-arsenobenzene - Google Patents
Improvements in or relating to the manufacture of 3.3-dichloro-4.4-dihydroxy-5.5-diacetylamino-arsenobenzeneInfo
- Publication number
- GB330862A GB330862A GB32524/29A GB3252429A GB330862A GB 330862 A GB330862 A GB 330862A GB 32524/29 A GB32524/29 A GB 32524/29A GB 3252429 A GB3252429 A GB 3252429A GB 330862 A GB330862 A GB 330862A
- Authority
- GB
- United Kingdom
- Prior art keywords
- dihydroxy
- dichloro
- arsenobenzene
- diacetylamino
- relating
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 238000004519 manufacturing process Methods 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 2
- CUVXIBDVSAFYDY-UHFFFAOYSA-N ClC=1C=C(C=C(C1O)[N+](=O)[O-])[AsH](O)=O Chemical compound ClC=1C=C(C=C(C1O)[N+](=O)[O-])[AsH](O)=O CUVXIBDVSAFYDY-UHFFFAOYSA-N 0.000 abstract 1
- -1 Organo arsenic Chemical compound 0.000 abstract 1
- 230000000397 acetylating effect Effects 0.000 abstract 1
- 229910052785 arsenic Inorganic materials 0.000 abstract 1
- 239000007858 starting material Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/66—Arsenic compounds
- C07F9/70—Organo-arsenic compounds
- C07F9/74—Aromatic compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Indole Compounds (AREA)
Abstract
330,862. I. G. Farbenindustrie Akt.- Ges. Oct. 25, 1928, [Convention date]. Addition to 296,327. Organo arsenic; compounds. - 3: 3<1>-Dichloro- 4 : 4<1>-,dihydroxy-5 : 5<1>-diacetylaminoarsenobenzene is prepared by acetylating the diamino compound. An example is given. The starting material is obtained by reducing 3-chloro-4-hydroxy-5-nitrophenylarsinic acid.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE330862X | 1928-10-25 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB330862A true GB330862A (en) | 1930-06-19 |
Family
ID=6193134
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB14343/27A Expired GB296327A (en) | 1928-10-25 | 1927-05-27 | Manufacture of new substituted 4.4-dihydroxy-5:5-acylamino-arsenobenzenes |
GB32524/29A Expired GB330862A (en) | 1928-10-25 | 1929-10-25 | Improvements in or relating to the manufacture of 3.3-dichloro-4.4-dihydroxy-5.5-diacetylamino-arsenobenzene |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB14343/27A Expired GB296327A (en) | 1928-10-25 | 1927-05-27 | Manufacture of new substituted 4.4-dihydroxy-5:5-acylamino-arsenobenzenes |
Country Status (1)
Country | Link |
---|---|
GB (2) | GB296327A (en) |
-
1927
- 1927-05-27 GB GB14343/27A patent/GB296327A/en not_active Expired
-
1929
- 1929-10-25 GB GB32524/29A patent/GB330862A/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
GB296327A (en) | 1928-08-27 |
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