CAS: 138-42-1; 4-Nitrobenzenesulfonic Acid

该化合物是一种芳香磺酸,其特点是硝基磺酸组和附在苯环上的磺酸组,其分子式为C6H6N2O4S,其成分为磺酸(-SO3H)组,该组具有强酸性,在水和极溶剂中溶解,硝基苯乙酸(-NO2)有助于其再活动,特别是在电益替代反应中.该化合物一般是黄色至褐色的固体,因其在有机合成中使用而闻名,特别是用作染料和药物的试剂.此外,该化合物可以用作硝酸剂,并用于各种工业用途.由于其酸性性质,还可在某些化学反应中起到催化剂作用.在处理该化合物时,应当采取安全防范措施,因为如果摄取或吸入,可能会造成伤害,并可能造成皮肤和眼刺激.

结构式图片

欧盟法规

ECHA物质ECHA物质C&L通报REACH预注册

上下游产品

di(p-nitrophenyl) disulfide nitrobenzene benzenesulfonic acid 4-aminobenzene sulfonic acid 4-nitro-benzenesulfonic acid-(4-bromo-phenacyl ester) 3-aminobenzenesulfonic acid 4-aminobenzene sulfonic acid 4,4'-hydrazo-bis-benzenesulfonic acid

合成工艺路线路线简述

    对氨基苯磺酸置于双氧水体系中,用 溶剂黄146 用作溶剂,化学反应 3.75H,反应生成4-硝基苯磺酸
    参考文献:Vincent,M.,Bulletin De La Societe Chimique De France,1962,P. 1587-1591
    标题:Vincent,M.,Bulletin De La Societe Chimique De France,1962,P. 1587-1591

    专利信息


    专利号:US-11926589-B2
    优先权日:2019-07-09
    标 题 :Process for the synthesis of non-racemic cyclohexenes
    发明人:REISMAN SARAH; ROMBOLA MICHAEL; LADD CAROLYN L; MCLAUGHLIN MARTIN JOHN; ZUEND STEPHAN; GOETZ ROLAND
    权利人:BASF CORP; CALIFORNIA INST OF TECHN
    摘要:This invention relates to a process for the synthesis of a non-racemic cyclohexene compound of formula (I) by a Diels-Alder reaction of a compound of formula (II) with a compound of formula (III) wherein R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 and Y have the meanings as defined in the description in the presence of a catalyst comprising at least one m-valent metal cation M m+ wherein the metal M is selected from Scandium (Sc), Yttrium (Y), Lanthanum (La), Cerium (Ce), Praseodymium (Pr), Neodymium (Nd), Promethium (Pm), Samarium (Sm), Europium (Eu), Gadolinium 15 (Gd), Terbium (Tb), Dysprosium (Dy), Holmium (Ho), Erbium (Er), Thulium (Tm), Ytterbium (Yb), Lutetium (Lu), Gallium (Ga) and Indium (In), and m is an integer of 1, 2 or 3, and a chiral ligand of the formula (IV) wherein R 10a , R 10b , R 10c , R 10d , R 10a′ , R 10b′ , R 10c′ , R 10d′ , Z and Z′ have the meanings as defined in the description.

    专利号:US-11548898-B2
    优先权日:2017-07-06
    标题 :Synthesis of halichondrins
    发明人:KISHI YOSHITO; AI YANRAN; YE NING; WANG QIAOYI; YAHATA KENZO; ISO Kentaro; NAINI SANTHOSH REDDY; YAMASHITA SHUJI; LEE JIHOON; OHASHI ISAO; FUKUYAMA TAKASHI
    权利人:HARVARD COLLEGE; EISAI R&D MAN CO LTD
    摘要:The present invention provides methods for the synthesis of ketones involving a Ni/Zr-mediated coupling reaction. The Ni/Zr-mediated ketolization reactions can be used in the synthesis of halichondrins (e.g., halichondrin A, B, C; homohalichondrin A, B, C; norhalichondrin A, B, C), and analogs thereof. Therefore, the present invention also provides synthetic methods useful for the synthesis of halichondrins, and analogs thereof. Also provided herein are compounds (i.e., intermediates) useful in the synthesis of halichondrins, and analogs thereof. In particular, the present invention provides methods and compounds useful in the synthesis of compound of Formula (H3-A).

    专利号:US-4287123-A
    优先权日:1980-01-14
    标题 :Synthesis of thienamycin via (3SR, 4RS)-3-((RS)-1-acyloxyethyl)-2-oxo-4-azetidineacetate
    发明人:LIU THOMAS M H; MELILLO DAVID G; RYAN KENNETH M; SHINKAI ICHIRO; SLETZINGER MEYER
    权利人:MERCK & CO INC
    摘要:Disclosed is a process for the stereocontrolled total synthesis of thienamycin, which synthesis proceeds via intermediate II: II wherein R is a readily removable carboxyl protecting group; and is a readily removable acyl group.

    专利号:US-4282148-A
    优先权日:1980-01-14
    标 题:Synthesis of thienamycin via esters of (3SR, 4RS)-3-[(SR)-1-hydroxyethyl]-β,2-dioxo-4-azetidinebutanoic acid
    发明人:LIU THOMAS M H; MELILLO DAVID G; RYAN KENNETH M; SHINKAI ICHIRO; SLETZINGER MEYER
    权利人:MERCK & CO INC
    摘要:Disclosed is a process for the stereocontrolled total synthesis of thienamycin, which synthesis proceeds via intermediate II: II wherein R3 is a readily removable carboxyl protecting group.

    专利号:US-4414155-A
    优先权日:1980-01-14
    标题 :Synthesis of thienamycin via esters of (3SR, 4RS)-3-[(SR)-1-hydroxyethyl]-β,2-dioxo-4-azetidinebutanoic acid
    发明人:LIU THOMAS M H; MELILLO DAVID G; RYAN KENNETH M; SHINKAI ICHIRO; SLETZINGER MEYER
    权利人:MERCK & CO INC
    摘要:Disclosed is a process for the stereocontrolled total synthesis of thienamycin, which synthesis proceeds via intermediate II: II wherein R3 is a readily removable carboxyl protecting group.

    专利号:US-4269772-A
    优先权日:1980-01-14
    标 题 :Synthesis of thienamycin via trans-3-carboxymethylene-4-carboxy-5-methyl-Δ2 -isoxazoline
    发明人:MELILLO DAVID G; RYAN KENNETH M
    权利人:MERCK & CO INC
    摘要:Disclosed is a process for the stereocontrolled total synthesis of thienamycin, which synthesis proceeds via intermediate II: II wherein R5 and R6 are removable protecting groups.
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    合成参考文献


    参考文献:10.1021/ol020037j
    摘要:Mulder JA, Hsung RP, Frederick MO, Tracey MR, Zificsak CA. The first stereoselective Ficini-Claisen rearrangement using chiral ynamides. Org Lett. 2002 Apr 18;4(8):1383–6. doi: 10.1021/ol020037j.
    参考文献:10.1107/s1600536810021379
    摘要:Al-Dajani MT, Abdallah HH, Mohamed N, Quah CK, Fun HK. Triethyl-ammonium 4-nitro-benzene-sulfonate. Acta Crystallogr Sect E Struct Rep Online. 2010 Jun 16;66(Pt 7):o1647.
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