{"type":"standard","title":"Chizuko Takahashi","displaytitle":"Chizuko Takahashi","namespace":{"id":0,"text":""},"wikibase_item":"Q5102671","titles":{"canonical":"Chizuko_Takahashi","normalized":"Chizuko Takahashi","display":"Chizuko Takahashi"},"pageid":11312105,"thumbnail":{"source":"https://upload.wikimedia.org/wikipedia/commons/thumb/a/ac/Chizuko_Takahashi_20221205hyoukei_0.jpg/330px-Chizuko_Takahashi_20221205hyoukei_0.jpg","width":320,"height":426},"originalimage":{"source":"https://upload.wikimedia.org/wikipedia/commons/a/ac/Chizuko_Takahashi_20221205hyoukei_0.jpg","width":335,"height":446},"lang":"en","dir":"ltr","revision":"1288234886","tid":"e183f266-2676-11f0-bc89-c0b2a428bf18","timestamp":"2025-05-01T10:27:28Z","description":"Japanese politician","description_source":"local","content_urls":{"desktop":{"page":"https://en.wikipedia.org/wiki/Chizuko_Takahashi","revisions":"https://en.wikipedia.org/wiki/Chizuko_Takahashi?action=history","edit":"https://en.wikipedia.org/wiki/Chizuko_Takahashi?action=edit","talk":"https://en.wikipedia.org/wiki/Talk:Chizuko_Takahashi"},"mobile":{"page":"https://en.m.wikipedia.org/wiki/Chizuko_Takahashi","revisions":"https://en.m.wikipedia.org/wiki/Special:History/Chizuko_Takahashi","edit":"https://en.m.wikipedia.org/wiki/Chizuko_Takahashi?action=edit","talk":"https://en.m.wikipedia.org/wiki/Talk:Chizuko_Takahashi"}},"extract":"Chizuko Takahashi is a Japanese politician and member of House of Representatives for the Japanese Communist Party.","extract_html":"
Chizuko Takahashi is a Japanese politician and member of House of Representatives for the Japanese Communist Party.
"}{"fact":"The most traveled cat is Hamlet, who escaped from his carrier while on a flight. He hid for seven weeks behind a panel on the airplane. By the time he was discovered, he had traveled nearly 373,000 miles (600,000 km).","length":217}
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{"slip": { "id": 171, "advice": "If you've nothing nice to say, say nothing."}}
{"type":"standard","title":"1-Aminoethanol","displaytitle":"1-Aminoethanol","namespace":{"id":0,"text":""},"wikibase_item":"Q18205235","titles":{"canonical":"1-Aminoethanol","normalized":"1-Aminoethanol","display":"1-Aminoethanol"},"pageid":43552180,"thumbnail":{"source":"https://upload.wikimedia.org/wikipedia/commons/thumb/a/a3/1-Aminoethanol.png/330px-1-Aminoethanol.png","width":320,"height":269},"originalimage":{"source":"https://upload.wikimedia.org/wikipedia/commons/a/a3/1-Aminoethanol.png","width":407,"height":342},"lang":"en","dir":"ltr","revision":"1191679874","tid":"98bf624b-a2c5-11ee-9084-84367ba218d1","timestamp":"2023-12-25T01:33:25Z","description":"Chemical compound","description_source":"local","content_urls":{"desktop":{"page":"https://en.wikipedia.org/wiki/1-Aminoethanol","revisions":"https://en.wikipedia.org/wiki/1-Aminoethanol?action=history","edit":"https://en.wikipedia.org/wiki/1-Aminoethanol?action=edit","talk":"https://en.wikipedia.org/wiki/Talk:1-Aminoethanol"},"mobile":{"page":"https://en.m.wikipedia.org/wiki/1-Aminoethanol","revisions":"https://en.m.wikipedia.org/wiki/Special:History/1-Aminoethanol","edit":"https://en.m.wikipedia.org/wiki/1-Aminoethanol?action=edit","talk":"https://en.m.wikipedia.org/wiki/Talk:1-Aminoethanol"}},"extract":"1-Aminoethanol is an organic compound with the formula CH3CH(NH2)OH. It is classified as an alkanolamine. Specifically, it is a structural isomer of 2-aminoethanol (ethanolamine). These two compounds differ in the position of the amino group. Since the central carbon atom in 1-aminoethanol has four different substituents, the compound has two stereoisomers. Unlike 2-aminoethanol, which is of considerable importance in commerce, 1-aminoethanol is not encountered as a pure material and is mainly of theoretical interest.","extract_html":"
1-Aminoethanol is an organic compound with the formula CH3CH(NH2)OH. It is classified as an alkanolamine. Specifically, it is a structural isomer of 2-aminoethanol (ethanolamine). These two compounds differ in the position of the amino group. Since the central carbon atom in 1-aminoethanol has four different substituents, the compound has two stereoisomers. Unlike 2-aminoethanol, which is of considerable importance in commerce, 1-aminoethanol is not encountered as a pure material and is mainly of theoretical interest.
"}{"slip": { "id": 124, "advice": "Do not check work email on your days off."}}
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