- 英文名称1,5-Diamino-4,8-Dihydroxyanthracene-9,10-Dione
- 中文名称1,5-二氨基-4,8-二羟基-9,10-蒽二酮
- IUPAC名称1,5-diamino-4,8-dihydroxyanthracene-9,10-dione
- 其它别名1,5-二氨基-4,8-二羟基蒽醌; 1,5-Dihydroxy-4,8-Diaminoanthraquinone
- CAS编号145-49-3
- MFCD编号:MFCD00013722
- EINECS号:205-655-8
- FDA UNII编号:Q7YVG56Q18
- 分子式:C14H10N2O4
- 分子量:270.24
- 产品CID: 690196
- 产品分类有机原料→分子砌块→芳环类化合物→苯类化合物
相似化合物
116-82-5 16517-70-7 116-85-8欧盟法规
ECHA物质C&L通报REACH预注册上下游产品
CAS号128-91-6 1,5-二羟基-4,8-二硝基蒽醌 | CAS号129-44-2 1,5-二氨基蒽醌 | CAS号82-35-9 1,5-二硝基蒽醌 | CAS号60080-32-2 1,5-bis(hydroxy... | CAS号85192-94-5 1,5-diazido-ant... | CAS号128-86-9 溶剂蓝74 | CAS号7664-93-9 硫酸 | CAS号7732-18-5 水 | CAS号7647-01-0 盐酸 | CAS号3860-63-7 分散蓝26 | CAS号100-39-0 溴化苄 | CAS号23478-60-6 1,4,5,8,9,10-An... | CAS号81-60-7 1,4,5,8-四羟基蒽醌 | CAS号117-12-4 蒽绛酚 | CAS号5138-23-8 2-Anthracenesul... | CAS号6370-58-7 N-(5-benzamido-... | CAS号6374-78-3 1-amino-4,5,8-t...1,5-Diazido-Anthraquinone置于硫酸体系中,化学反应生成1,5-二氨基-4,8-二羟基-9,10-蒽二酮
参考文献:Brass; Albrecht,Chemische Berichte,1928,Vol. 61,P. 988
标题:Brass; Albrecht,Chemische Berichte,1928,Vol. 61,P. 988
海关参考信息
- 2912110000-甲醛
2912210000-苯甲醛
2914610000-蒽醌
2907121100-间甲酚 - 💡 提示:海关信息按照顺序优先匹配,如需确认的海关信息,请参考相关资料。
- 详情请参考:📖 海关编码查询和海关进出口税则
专利信息
专利号:CN-101054681-A
优先权日:2007-02-14
标题:Method for one-step electrolytic synthesis of 1,5-diamino-4,8-dihydroxyanthraquinone
专利号:US-4045457-A
优先权日:1974-10-23
标题:Anthraquinone dyestuffs
发明人:GEHRKE GUNTER; SCHMITZ REINOLD; BIEN HANS-SAMUEL; HERZOG HELMUT
权利人:BAYER AG
摘要:The invention relates to a process for the preparation of water-insoluble chlorine-containing diaminodihydroxyanthraquinone dyestuffs. The process consists in that 2,8-dichloro-1,5-dinitroanthraquinone and/or 2,5-dichloro-1,8-dinitroanthraquinone is warmed with sulphur in concentrated sulphuric acid having a maximum SO 3 content of 20% - possibly in the presence of boric acid - the resulting compounds are, if appropriate, post-halogenated and/or alkylated, preferably in the same reaction batch. n The main advantage of this process is that it starts from 1,6- and/or 1,7-dichloroanthraquinone, for which there was hitherto no industrial use, but which unavoidably also arise during the synthesis 1,5- and 1,8-dichloroanthraquinones.