Huahana Huahana
Ka nana aku | Paʻa keʻokeʻo a keʻokeʻo |
Ka hoʻololi kikoʻī[α]20/D (C=2, Ethanol) | -103.0° a i -109.0° |
Wai(KF) | Ma lalo o 1.0% |
MP | 95.0-103.0 ℃ |
Maʻemaʻe (HPLC) | ʻoi aku ma mua o 98.0% |
Maʻemaʻe kiral | ʻoi aku ma mua o 99.0% |
Hoʻāʻo | 97.0% -101.0% |
Manawa mana | 2 makahiki |
Pūʻolo | 25kg/ pahu |
Kaʻahele | ma ke kai a ma ka lewa a ma ka ʻāina |
ʻĀina i kumu | Kina |
ʻŌlelo uku | T/T |
Nā huaʻōlelo like
2-PYRROLIDINECARBOXAMIDE, (2S)-
H-PRO-NH2
L-(-)-PROLINAMIDE
L-PROLINE AMIDE
L-PYRROLIDINE-2-CARBOXYLIC ACID AMIDE
PROLINAMIDE
PROLINE-NH2
(S)-PROLINAMIDE
(S)-PYRROLIDINE-2-CARBOXYLIC ACID AMIDE
(s)-(-)-pyrrolidin-2-carbonsaeureamid
(S)-pyrrolidine-2-carboxamide
L-PROLINAMIDE BASE FREE
Pro-Nh2
H-Pro-NH2, kumu manuahi
HL-Pro-NH2
(S)-2-Pyrrolidinecarboxamide
L-Srolinamide, 98%
L-Pro-NH2
Palapala noi
Hiki ke hoʻohana ʻia ʻo L-prolineamide ma ke ʻano he kumu waiwai o nā huahana olakino, nā lāʻau lapaʻau a me nā intermediates vidaletin.
ʻO L-prolineamide kekahi mea nui o ka optically active pyrrole derivative, hiki ke hoʻopili pololei i ka asymmetric Robinson cyclization o ka puke kemika a me ka hopena aldol.
He mea koʻikoʻi ka L-prolineamide i ka peptide synthesis a hiki ke hoʻohana ʻia ma ke ʻano he chiral intermediate e synthesize i kekahi mau lāʻau chiral.
Kiekie
1. Loaʻa iā mākou ka pae ton i ka waihona, a hiki iā mākou ke hāʻawi koke i ka mea ma hope o ka loaʻa ʻana o ke kauoha.
2. Hiki ke hāʻawi ʻia ke kumukūʻai kiʻekiʻe & hoʻokūkū.
3.Quality analysis report (COA) o ka pahu hoʻouna e hāʻawi ʻia ma mua o ka hoʻouna ʻana.
4. Hiki ke hā'awi 'ia ka nīnau nīnau mea kū'ai a me nā palapala 'ike loea inā noi ma hope o ka hālāwai 'ana i kekahi huina.
5. Nui ma hope o ke kūʻai aku a hōʻoiaʻiʻo paha: E hoʻoponopono koke ʻia kekahi o kāu nīnau.
6. E hoʻokuʻu aku i nā huahana hoʻokūkū a hoʻokuʻu aku iā lākou i nā ʻāina ʻē i ka nui o kēlā me kēia makahiki.