| 规格 | 目录价格 | 上海 | 安徽 | 武汉 | 成都 | 北方 | 深圳 | 会员价格 | 数量 |
|---|---|---|---|---|---|---|---|---|---|
| 1g | ¥ ưźʼnĽĽ | > 1 | > 1 | -- | 1 | 1 | -- | ¥ ưźʼnĽĽ | - + |
| 5g | ¥ ưƞʼnĽĽ | > 1 | > 1 | -- | 1 | 2 | -- | ¥ ưƞʼnĽĽ | - + |
| 1g | ¥ ưǯʼnĽĽ | > 1 | > 1 | 1 | 3 | -- | ¥ ưǯʼnĽĽ | - + | |
| 25g | ¥ ŢȀʼnĽĽ | > 1 | > 1 | 7 | > 1 | > 1 | > 1 | ¥ ŢȀʼnĽĽ | - + |
| 1g | ¥ ȎŢĽʼnĽĽ | > 1 | > 1 | -- | > 1 | > 1 | 6 | ¥ ȎŢĽʼnĽĽ | - + |
| 5g | ¥ ƞƄŔʼnĽĽ | > 1 | > 1 | 3 | 6 | 7 | ¥ ƞƄŔʼnĽĽ | - + | |
| 1kg | ¥ ȎưŔǯʼnĽĽ | > 1 | > 1 | -- | 9 | -- | ¥ ȎưŔǯʼnĽĽ | - + | |
| 大货 | 请询价 | -- | -- | -- | -- | -- | -- | -- | - + |
77.32
[1]. Masahiro Terada, et al. Axially chiral guanidine as highly active and enantioselective catalyst for electrophilic amination of unsymmetrically substituted 1,3-dicarbonyl compounds. J Am Chem Soc. 26 Dec 2;128(5):16-5.
[2]. Masaru Kondo, et al. Catalytic Enantioselective Reaction of α-Aminoacetonitriles Using Chiral Bis(imidazoline) Palladium Catalysts. Angew Chem Int Ed Engl. 215 Jul 6;5(28):8198-22.
[3]. Sebastian Brandes, et al. Chirally aminated 2-naphthols--organocatalytic synthesis of non-biaryl atropisomers by asymmetric Friedel-Crafts amination. Angew Chem Int Ed Engl. 26 Feb 6;5(7):117-51.

P21-P261-P26-P271-P28-P32+P352-P3+P3-P362-P37+P378-P51
GHS2,GHS7
.1
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