(3S,2S)-2,3-Diaminobutyric acid 2HCl
Base Information
- Chemical Name: (3S,2S)-2,3-Diaminobutyric acid 2HCl
- CAS No.: 121054-30-6
Chinese Manufacturer supply (3S,2S)-2,3-Diaminobutyric acid 2HCl 121054-30-6 in stock with high standard
- Molecular Formula: C4H10N2O2*2ClH
- Molecular Weight: 191.057
- PSA： 89.34000
- LogP: 1.75010
121054-30-6 Relevant articles
Nine enzymes are required for assembly of the pacidamycin group of peptidyl nucleoside antibiotics
Zhang, Wenjun,Ntai, Ioanna,Bolla, Megan L.,Malcolmson, Steven J.,Kahne, Daniel,Kelleher, Neil L.,Walsh, Christopher T.
supporting information; experimental part, p. 5240 - 5243 (2011/06/17)
Pacidamycins are a family of uridyl pept...
Stereocontrolled route to vicinal diamines by [3.3] sigmatropic rearrangement of allyl cyanate: Asymmetric synthesis of anti-(2R,3R)- and syn-(2R,3S)-2,3-diaminobutanoic acids
Ichikawa, Yoshiyasu,Egawa, Haruka,Ito, Takashi,Isobe, Minoru,Nakano, Keiji,Kotsuki, Hiyoshizo
, p. 5737 - 5740 (2007/10/03)
(Diagram presented) A stereocontrolled r...
New synthesis and ring opening of cis-3-alkylaziridine-2-carboxylates
Lee, Kwang-Deuk,Suh, Jang-Min,Park, Jae-Hoon,Ha, Hyun-Joon,Choi, Hwan Gun,Park, Chan Sun,Chang, Jae Won,Lee, Won Koo,Dong, Yongkwan,Yun, Hoseop
, p. 8267 - 8276 (2007/10/03)
Syntheses of cis-3-alkylaziridine-2-carb...
Asymmetric hydrogenation of (E)-α, β-bis(N-acylamino)acrylates catalyzed by a rhodium complex with trans-chelating chiral diphosphine ligand
Kuwano, Ryoichi,Okuda, Satoshi,Ito, Yoshihiko
, p. 2773 - 2775 (2007/10/03)
The asymmetric hydrogenation of (E)-α,β-...
121054-30-6 Process route
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-
(4R,5R)-1-benzyl 4-carbomethoxy-3-ethanoyl-5-methyl-2-oxoimidazolidine-1-carboxylate
-
-
121054-30-6,648922-13-8
(2R,3R)-2,3-diaminobutanoic acid dihydrochloride
| Conditions | Yield |
|---|---|
|
With
hydrogenchloride;
In
water;
at 90 ℃;
for 24h;
|
89%
|
-
-
917839-23-7
(4R,5S)-1-benzyl 4-carbomethoxy-3-ethanoyl-5-methyl-2-oxoimidazolidine-1-carboxylate
-
-
121054-30-6,648922-13-8
(2R,3S)-2,3-diaminobutanoic acid dihydrochloride
| Conditions | Yield |
|---|---|
|
With
hydrogenchloride;
In
water;
at 90 ℃;
for 24h;
|
92%
|
121054-30-6 Upstream products
-
917839-23-7
(4R,5S)-1-benzyl 4-carbomethoxy-3-ethanoyl-5-methyl-2-oxoimidazolidine-1-carboxylate
-
215652-47-4
(2S,3R)-2-Acetylamino-3-benzyloxycarbonylamino-butyric acid methyl ester
-
389631-23-6
ethyl (2S,3R)-2,3-bis-N-tert-butoxycarbonylamino butanoate