홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

2,6-Difluorobenzoyl isocyanate → Teflubenzuron

HRID 1462014
노트
인쇄 미리보기

반응식

HRID 1462014 반응식
[F:1][C:2]1[CH:12]=[CH:11][CH:10]=[C:9]([F:13])[C:3]=1[C:4]([N:6]=[C:7]=[O:8])=[O:5].[F:14][C:15]1[C:21]([Cl:22])=[C:20]([F:23])[C:19]([Cl:24])=[CH:18][C:16]=1[NH2:17]>C1(C)C=CC=CC=1>[F:14][C:15]1[C:21]([Cl:22])=[C:20]([F:23])[C:19]([Cl:24])=[CH:18][C:16]=1[NH:17][C:7]([NH:6][C:4](=[O:5])[C:3]1[C:2]([F:1])=[CH:12][CH:11]=[CH:10][C:9]=1[F:13])=[O:8]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 27333692,6-Difluorobenzoyl isocyanateHCID 27740003,5-Dichloro-2,4-difluorobenzenamine

생성물 1

HCID 91734Teflubenzuron

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

Three grams (0.016 mol) of 2,6-difluoro-benzoyl isocyanate were added to a solution of 2.95 gm (0.015 mol) of 2,4-difluoro-3,5-dichloroaniline in 50 ml of toluene. The solution thus obtained was stirred for 15 hours at room temperature. Thereafter, the product which precipitated during that time was removed by suction filtration and dried.

후처리

  1. customThe solution thus obtained
이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  • customThereafter, the product which precipitated during that time
  • customwas removed by suction filtration
  • customdried
  • 출처 및 근거

    ORD 기록
    ord-9bf4f69978b74406ae77f12ebb41fc96
    출처 데이터셋
    uspto-grants-1984_07
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04457943

    반응 노트

    불러오는 중…