GB331459A - - Google Patents

Info

Publication number

GB331459A

GB331459A GB31832/29A GB3183229A GB331459A GB 331459 A GB331459 A GB 331459A GB 31832/29 A GB31832/29 A GB 31832/29A GB 3183229 A GB3183229 A GB 3183229A GB 331459 A GB331459 A GB 331459A

Authority

GB

United Kingdom

Prior art keywords

groups

naphthol

developed

tartaric acid

diazo

Prior art date

1928-10-19

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

• Espacenet
• Global Dossier
• Discuss

• JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 abstract 4
• FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 abstract 3
• 235000002906 tartaric acid Nutrition 0.000 abstract 3
• 239000011975 tartaric acid Substances 0.000 abstract 3
• QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 abstract 2
• FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 abstract 2
• ZRALSGWEFCBTJO-UHFFFAOYSA-N guanidine group Chemical group NC(=N)N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 abstract 2
• -1 hydroxy aryl guanidines Chemical class 0.000 abstract 2
• 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 2
• 239000000203 mixture Substances 0.000 abstract 2
• 150000003839 salts Chemical class 0.000 abstract 2
• UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 abstract 2
• 235000005074 zinc chloride Nutrition 0.000 abstract 2
• 239000011592 zinc chloride Substances 0.000 abstract 2
• OFRMTRNULBCTHS-UHFFFAOYSA-N 2-[2-[2-[2-[bis(carboxymethyl)amino]-5-(2-diazoacetyl)phenoxy]ethoxy]-N-(carboxymethyl)-4-(2-diazoacetyl)anilino]acetic acid Chemical compound C(=O)(O)CN(C1=C(OCCOC2=C(C=CC(=C2)C(C=[N+]=[N-])=O)N(CC(=O)O)CC(=O)O)C=C(C=C1)C(C=[N+]=[N-])=O)CC(=O)O OFRMTRNULBCTHS-UHFFFAOYSA-N 0.000 abstract 1
• DHACJVAMAJZUFP-UHFFFAOYSA-N 4-N-(diazomethyl)-4-N-methylbenzene-1,4-diamine Chemical compound [N+](=[N-])=CN(C1=CC=C(C=C1)N)C DHACJVAMAJZUFP-UHFFFAOYSA-N 0.000 abstract 1
• DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 abstract 1
• XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Natural products NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 abstract 1
• 125000002252 acyl group Chemical group 0.000 abstract 1
• 239000003513 alkali Substances 0.000 abstract 1
• WDIHJSXYQDMJHN-UHFFFAOYSA-L barium chloride Chemical compound [Cl-].[Cl-].[Ba+2] WDIHJSXYQDMJHN-UHFFFAOYSA-L 0.000 abstract 1
• 229910001626 barium chloride Inorganic materials 0.000 abstract 1
• 229910021538 borax Inorganic materials 0.000 abstract 1
• 150000008049 diazo compounds Chemical class 0.000 abstract 1
• 229910052708 sodium Inorganic materials 0.000 abstract 1
• 239000011734 sodium Substances 0.000 abstract 1
• 239000004328 sodium tetraborate Substances 0.000 abstract 1
• 235000010339 sodium tetraborate Nutrition 0.000 abstract 1
• 239000000126 substance Substances 0.000 abstract 1

Cited By (2)