其它产品项目整合

项目整合的本质是一项集合成方法学、反应工程学与过程分析技术于一体的系统工程。其核心逻辑可以概括为以下几点：源头优选：利用如N-硝胺化学等底层方法学突破，从分子层面颠覆传统高成本、高污染路线。过程强化：依托连续流技术，攻克有机金属试剂应用、光化学反应放大等“不可能”任务，实现高危工艺的本质安全。系统集成：整合“反应-淬灭-分离”全流程，利用微流控与在线分析技术，消除批次间的差异，实现药品制造的连续化与智能化。当前，中间体工艺研发正在经历从“经验驱动”向“数据驱动”的转变。AI辅助路线设计、自动化高通量筛选与连续制造平台的结合，将使得“分子结构与最优工艺路径”之间的映射关系逐渐清晰。未来的竞争优势，将属于那些能够将底层化学创新与先进工程技术进行无缝整合的研发体系。
备注: 根据相关法律法规, 本站点不显示有法律约束管制的产品, 如有遗漏, 请自行鉴别,或提交我们及时更新撤除.
如有产品相关项目调研推广服务, 请致函联系我们

客户展示

其它产品项目整合

Fenoxazoline CAS Registry Number: 4846-91-7 非诺唑啉

CAS Name: 4,5-Dihydro-2-[[2-(1-methylethyl)phenoxy]methyl]-1H-imidazole
Additional Names: 2-[(o-cumenyloxy)methyl]-2-imidazoline; 2-(o-isopropylphenoxymethyl)-2-imidazoline; phenoxazoline
Pe...
Literature References: Preparation: FR 1365971 (1964 to Lab. Dausse and Soc. BMC). Use as sympathomimetic agent: Giudicelli, US 3198703 (1965 to Lab. Dausse).

Leiopyrrole CAS Registry Number: 5633-16-9 利奥吡咯

CAS Name: N,N-Diethyl-2-[2-(2-methyl-5-phenyl-1H-pyrrol-1-yl)phenoxy]ethanamine
Additional Names: 1-[o-(2-diethylaminoethoxy)phenyl]-2-methyl-5-phenylpyrrole; 2-methyl-1-(2-b-diethylaminoethoxy...
Literature References: Preparation: Buu-Hoi et al., J. Med. Pharm. Chem. 1, 23 (1959).

Dodecarbonium Chloride CAS Registry Number: 100-95-8 美他氯铵

CAS Name: N-[2-(Dodecylamino)-2-oxoethyl]-N,N-dimethylbenzenemethanaminium chloride
Additional Names: benzyl[(dodecylcarbamoylmethyl)dimethyl]ammonium chloride; N,N-dimethyl-N-benzyl-N-chloro-N...
Literature References: Preparation: Hentrich et al., US 2295655 (1942 to Patchem, AG).

N-Methylmyosmine CAS Registry Number: 525-74-6 3-(4,5-二氢-1-甲基-1H-吡咯-2-基)吡啶

CAS Name: 3-(4,5-Dihydro-1-methyl-1H-pyrrol-2-yl)pyridine
Additional Names: N-methyl-2-(3-pyridyl)-2-pyrroline; 4,5-dihydro-b-nicotyrine
Percent Composition: C 74.96%, H 7.55%, N 17.48%
Literature References: Preparation: Korte, Schulze-Steinen, Ber. 95, 2444 (1962).

Cetyl Lactate CAS Registry Number: 35274-05-6 乳酸十六烷基酯

CAS Name: 2-Hydroxypropanoic acid hexadecyl ester
Additional Names: 1-hexadecanol lactate; lactic acid cetyl ester; lactic acid hexadecyl ester
Trademarks: Ceraphyl 28
Percent Composition...
Literature References: Preparation: Rehberg, Marion, J. Am. Chem. Soc. 72, 1918 (1950).

Nitrosyl Fluoride CAS Registry Number: 7789-25-5 亚硝酰氟

Additional Names: Nitrogen oxyfluoride
Percent Composition: F 38.77%, N 28.59%, O 32.65%
Literature References: Preparation: Ruff et al., Z. Anorg. Allg. Chem. 208, 293 (1932); Balz, Mailänder, ibid. 217, 166 (1934); Faloon, Kenna, J. Am. Chem. Soc. 73, 2937 (1951); Kwasnik in Handbook of Preparative Inorganic Chemistry vol. 1, G. Brauer, Ed. (Academic Press, New York, 2nd ed., 1963) pp 184-185. Reviews: Hoffman, Neville, Chem. Rev. 62, 1-18 (1962); Kemmitt, Sharp, Adv. Fluorine Chem. 4, 194-195 (1965); Woolf, ibid. 5, 1-30 (1965); Schmutzler, Angew. Chem. Int. Ed. 7, 440-455 (1968).

Potassium Hexachloroosmate(IV) CAS Registry Number: 16871-60-6 六氯锇酸钾

Additional Names: Osmium potassium chloride
Percent Composition: Cl 44.21%, K 16.25%, Os 39.54%
Literature References: Preparation: Turner et al., Anal. Chem. 30, 1708 (1958).

Potassium Tetrafluoroborate CAS Registry Number: 14075-53-7 氟硼酸钾

Additional Names: Potassium borofluoride; potassium fluoborate; avogadrite
Percent Composition: B 8.59%, F 60.36%, K 31.06%
Literature References: Prepared according to the eq H3BO3 + 4HF + KOH = KBF4 + 4H2O: Vorländer et al., Ber. 65, 535 (1932); Kwasnik in Handbook of Preparative Inorganic Chemistry vol. 1, G. Brauer, Ed. (Academic Press, New York, 2nd ed., 1963) p 223. For other methods of prepn see H. S. Booth, D. R. Martin, Boron Trifluoride and Its Derivatives (New York, 1949) pp 99-106.

Orange I CAS Registry Number: 523-44-4 α-萘酚橙

CAS Name: 4-[(4-Hydroxy-1-naphthalenyl)azo]benzenesulfonic acid monosodium salt
Additional Names: Tropaeolin OOO no. 1; C.I. Acid Orange 20; FD C Orange I; Ext. D C Orange 3; C.I. 14600; a-na...
Literature References: Prepared by coupling diazotized sulfanilic acid with a-naphthol: Colour Index vol. 4 (3rd ed., 1971) p 4065.

sym-Trinitrobenzene CAS Registry Number: 99-35-4 1,3,5-三硝基苯

CAS Name: 1,3,5-Trinitrobenzene
Additional Names: benzite
Percent Composition: C 33.82%, H 1.42%, N 19.72%, O 45.05%
Literature References: Prepared by decarboxylation of trinitrobenzoic acid, obtained by oxidation of TNT: Clarke, Hartman, Org. Synth. 2, 93 (1922); by the action of alkali on 2,4,6-trinitrobenzaldehyde: Secareanu, Bull. Soc. Chim. 51, 591 (1932). Use as explosive, less sensitive to impact than TNT but more powerful and brisant: Robertson, J. Chem. Soc. 119, 8 (1921); van Duin, Rec. Trav. Chim. 39, 687 (1920). Review of toxicology and human exposure: Toxicological Profile for 1,3-Dinitrobenzene and 1,3,5-Trinitrobenzene (PB95-264289, 1995) 168 p.