CAS No.27167-53-9,Z-D-ALA-OSU Suppliers

Dayang Chem (Hangzhou) Co.,Ltd.

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N-[(Phenylmethoxy)carbonyl]-D-alanine 2,5-dioxo-1-pyrrolidinyl ester

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Research Peptide Biotechnology Co., Ltd.

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D-Alanine,N-[(phenylmethoxy)carbonyl]-, 2,5-dioxo-1-pyrrolidinyl ester

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Henan Allgreen Chemical Co.,Ltd

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DIMETHYL BRASSYLATE

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Antimex Chemical Limied

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Henan Tianfu Chemical Co., Ltd.

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ZHEJIANG JIUZHOU CHEM CO.,LTD

factory?direct?saleAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:healing drugs Transportation:By sea Port:Shanghai/tianjin

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ENAO Chemical Co, Limited

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wuxi leji biology technology co., LTD

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Shanghai Apeptide Co., Ltd.

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Shanghai Run-Biotech Co., Ltd.

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NovaChemistry

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INDOFINE Chemical Company, Inc.

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Synthetic route

: 6066-82-6
1-hydroxy-pyrrolidine-2,5-dione

: 26607-51-2
N-benzyloxycarbonyl-D-alanine

: 27167-53-9
N-(benzyloxycarbonyl)-D-alanine N-hydroxysuccinimide ester

Conditions

Conditions	Yield
With dicyclohexyl-carbodiimide In acetonitrile at 0 - 20℃; for 12.5h;	85%
With dicyclohexyl-carbodiimide In acetonitrile at -20℃;	57%
With dicyclohexyl-carbodiimide In 1,4-dioxane for 12h; Ambient temperature;

: 74124-79-1
di(succinimido) carbonate

: 26607-51-2
N-benzyloxycarbonyl-D-alanine

: 27167-53-9
N-(benzyloxycarbonyl)-D-alanine N-hydroxysuccinimide ester

Conditions

Conditions	Yield
With triethylamine In N,N-dimethyl-formamide at 0℃; for 1h;

: 27167-53-9
N-(benzyloxycarbonyl)-D-alanine N-hydroxysuccinimide ester

: 13433-00-6
diethyl aminomalonate hydrochloride

: 130548-14-0
Z-D-Ala-Ama(OEt)-OEt

Conditions

Conditions	Yield
With triethylamine In chloroform Ambient temperature;	88.9%

: 27167-53-9
N-(benzyloxycarbonyl)-D-alanine N-hydroxysuccinimide ester

: 7533-40-6
(S)-2-amino-4-methylpentan-1-ol

: 177657-04-4
(2S)-2-[N-(Benzyloxycarbonyl-(R)-alanyl)amino]-4-methylpentan-1-ol

Conditions

Conditions	Yield
In 1,4-dioxane for 12h; Ambient temperature;	88%

: 27167-53-9
N-(benzyloxycarbonyl)-D-alanine N-hydroxysuccinimide ester

: 73995-22-9
(S)-4-Amino-4-(ethoxycarbonylmethyl-carbamoyl)-butyric acid tert-butyl ester

: 126027-24-5
Z-D-Ala-Glu(OBut)-Gly-OEt

Conditions

Conditions	Yield
With 4-methyl-morpholine In N,N-dimethyl-formamide for 8h; Ambient temperature;	76%

: 27167-53-9
N-(benzyloxycarbonyl)-D-alanine N-hydroxysuccinimide ester

: 184684-98-8
(S)-2-Amino-3-{4-[bis-(2-hydroxy-ethyl)-amino]-phenyl}-propionic acid benzyl ester

: 184685-00-5
N-(N-benzyloxycarbonyl-D-alanyl)-p-bis(2-hydroxyethyl)amino-L-phenylalanine benzyl ester

Conditions

Conditions	Yield
In 1,4-dioxane at 25℃; for 1.5h;	73%

: 27167-53-9
N-(benzyloxycarbonyl)-D-alanine N-hydroxysuccinimide ester

: 157-06-2
D-arginine

: Z-D-Ala-D-Arg-OH hydrochloride

Conditions

Conditions	Yield
Stage #1: N-(benzyloxycarbonyl)-D-alanine N-hydroxysuccinimide ester; D-arginine In water; acetonitrile at 20℃; Stage #2: With hydrogenchloride In water; acetonitrile pH=2.5;	73%

: 61-54-1
tryptamine

: 27167-53-9
N-(benzyloxycarbonyl)-D-alanine N-hydroxysuccinimide ester

: 940290-20-0
N-(benzyloxycarbonyl)-D-alanine tryptamide

Conditions

Conditions	Yield
In tetrahydrofuran at 20℃;	71%

: 27167-53-9
N-(benzyloxycarbonyl)-D-alanine N-hydroxysuccinimide ester

: 58651-64-2
(S)-(2-amino-4-(tert-butoxy)-4-oxobutanoyl)glycine

: 126027-23-4
Z-D-Ala-Asp(OBut)-Gly-OH

Conditions

Conditions	Yield
With 4-methyl-morpholine In N,N-dimethyl-formamide for 8h; Ambient temperature;	68%

: 27167-53-9
N-(benzyloxycarbonyl)-D-alanine N-hydroxysuccinimide ester

: 66068-76-6
(S)-1-aminoethylphosphonic acid

: 98820-76-9
[(S)-1-((R)-2-Benzyloxycarbonylamino-propionylamino)-ethyl]-phosphonic acid

Conditions

Conditions	Yield
With sodium hydrogencarbonate In ethanol; water	56%

: 27167-53-9
N-(benzyloxycarbonyl)-D-alanine N-hydroxysuccinimide ester

: 60687-36-7
(R)-(1-aminoethyl)phosphonic acid

: 98820-75-8
[(R)-1-((R)-2-Benzyloxycarbonylamino-propionylamino)-ethyl]-phosphonic acid

Conditions

Conditions	Yield
With sodium hydrogencarbonate In ethanol; water	41%

: 27167-53-9
N-(benzyloxycarbonyl)-D-alanine N-hydroxysuccinimide ester

: 22839-63-0
L-Glu-L-Phe-O-Me

: Z-D-Ala-L-Glu(OH)-L-Phe-O-Me

Conditions

Conditions	Yield
	28%

: 27167-53-9
N-(benzyloxycarbonyl)-D-alanine N-hydroxysuccinimide ester

: 6323-97-3
1-aminoethanephosphonic acid

A: 98820-75-8
[(R)-1-((R)-2-Benzyloxycarbonylamino-propionylamino)-ethyl]-phosphonic acid

B: 98820-76-9
[(S)-1-((R)-2-Benzyloxycarbonylamino-propionylamino)-ethyl]-phosphonic acid

Conditions

Conditions	Yield
With sodium hydrogencarbonate In ethanol; water	A 18% B 2%

...Expand

: 27167-53-9
N-(benzyloxycarbonyl)-D-alanine N-hydroxysuccinimide ester

: 7517-19-3
methyl (L)-leucinate hydrochloride

: 27167-66-4
Z-D-Ala-L-Leu-OMe

Conditions

Conditions	Yield
With triethylamine In chloroform

: 27167-53-9
N-(benzyloxycarbonyl)-D-alanine N-hydroxysuccinimide ester

: 1066-51-9
Aminomethylphosphonic acid

: [((R)-2-Benzyloxycarbonylamino-propionylamino)-methyl]-phosphonic acid

Conditions

Conditions	Yield
With sodium hydrogencarbonate In ethanol; water

: 27167-53-9
N-(benzyloxycarbonyl)-D-alanine N-hydroxysuccinimide ester

: (S)-3-Amino-N-((R)-1-methoxycarbonyl-ethyl)-succinamic acid benzyl ester

: Z-D-Ala-L-Asp(OBzl)-D-Ala-O-Me

Conditions

Conditions	Yield
With triethylamine In chloroform 1) ice bath, 1 h, 2) RT, 3 h + overnight; Yield given;

: 27167-53-9
N-(benzyloxycarbonyl)-D-alanine N-hydroxysuccinimide ester

: 65864-26-8
Z-Trp-Nle-Asp(OBzl)-Phe-NH2

: Z-D-Ala-Trp-Nle-Asp-Phe-NH2

Conditions

Conditions	Yield
With hydrogen; N-ethyl-N,N-diisopropylamine; palladium on activated charcoal 1.) DMF, AcOH, H2O, RT, 2.) DMF, 3 h, RT; Yield given. Multistep reaction;

: 27167-53-9
N-(benzyloxycarbonyl)-D-alanine N-hydroxysuccinimide ester

: 14047-23-5
1-aminopropanephosphonic acid

: [1-((R)-2-Benzyloxycarbonylamino-propionylamino)-propyl]-phosphonic acid

Conditions

Conditions	Yield
With triethylamine In ethanol

: 27167-53-9
N-(benzyloxycarbonyl)-D-alanine N-hydroxysuccinimide ester

: (1R,S)-1-(D-alanylamino)propanephosphonic acid

: {1-[(R)-2-((R)-2-Benzyloxycarbonylamino-propionylamino)-propionylamino]-propyl}-phosphonic acid

Conditions

Conditions	Yield
With triethylamine In ethanol

: 27167-53-9
N-(benzyloxycarbonyl)-D-alanine N-hydroxysuccinimide ester

: 27454-32-6
Z-D-Ala-NHNH-Boc

: 27454-33-7
Z-D-Ala-D-Ala-NHNH-Boc

Conditions

Conditions	Yield
(i) H2, PdO, (ii) /BRN= 1553989/; Multistep reaction;

: 27167-53-9
N-(benzyloxycarbonyl)-D-alanine N-hydroxysuccinimide ester

: 132832-29-2
7-<(2R,3S)-3-amino-2-methyl-1-azetidinyl>-1-cyclopropyl-1,4-dihydro-6-fluoro-4-oxo=1,8-naphthyridine-3-carboxylic acid

: 148496-72-4
7-<(2R,3S)-3-N-CBZ-D-Ala-amino-2-methyl-1-azetidinyl>-1-cyclopropyl-1,4-dihydro-6-fluoro-4-oxo-1,8-naphthyridine-3-carboxylic acid

Conditions

Conditions	Yield
With 4-methyl-morpholine In N,N-dimethyl-formamide for 8h; Ambient temperature;

: 27167-53-9
N-(benzyloxycarbonyl)-D-alanine N-hydroxysuccinimide ester

: 132832-30-5
7-<(2S,3R)-3-amino-2-methyl-1-azetidinyl>-1-cyclopropyl-1,4-dihydro-6-fluoro-4-oxo-1,8-naphthyridine-3-carboxylic acid

: 148496-71-3
7-<(2S,3R)-3-N-CBZ-D-Ala-amino-2-methyl-1-azetidinyl>-1-cyclopropyl-1,4-dihydro-6-fluoro-4-oxo-1,8-naphthyridine-3-carboxylic acid

Conditions

Conditions	Yield
With 4-methyl-morpholine In N,N-dimethyl-formamide for 8h; Ambient temperature;

: 27167-53-9
N-(benzyloxycarbonyl)-D-alanine N-hydroxysuccinimide ester

: 141725-88-4
cetefloxacin

: 7-[(2S,3R)-3-((R)-2-Benzyloxycarbonylamino-propionylamino)-2-methyl-azetidin-1-yl]-1-(2,4-difluoro-phenyl)-6-fluoro-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid

Conditions

Conditions	Yield
With 4-methyl-morpholine In N,N-dimethyl-formamide for 8h; Ambient temperature;

: 27167-53-9
N-(benzyloxycarbonyl)-D-alanine N-hydroxysuccinimide ester

: 111-40-0
1,5-diamino-3-azapentane

: ((R)-1-{2-[2-((R)-2-Benzyloxycarbonylamino-propionylamino)-ethylamino]-ethylcarbamoyl}-ethyl)-carbamic acid benzyl ester

Conditions

Conditions	Yield
With triethylamine In dichloromethane

: 27167-53-9
N-(benzyloxycarbonyl)-D-alanine N-hydroxysuccinimide ester

: (S)-2-Amino-3-{4-[bis-(2-hydroxy-ethyl)-amino]-phenyl}-propionic acid benzyl ester; hydrochloride

: 184685-00-5
N-(N-benzyloxycarbonyl-D-alanyl)-p-bis(2-hydroxyethyl)amino-L-phenylalanine benzyl ester

Conditions

Conditions	Yield
In 1,4-dioxane	2.2 g

: 27167-53-9
N-(benzyloxycarbonyl)-D-alanine N-hydroxysuccinimide ester

: 62-57-7
2-Aminoisobutyric acid

: 105590-88-3
N-phenylmethoxycarbonyl-D-alanyl-2-methylalanine

Conditions

Conditions	Yield
In N,N-dimethyl-formamide

: 27167-53-9
N-(benzyloxycarbonyl)-D-alanine N-hydroxysuccinimide ester

: 65733-15-5
(R)-2-amino-3-(4-(benzyloxy)phenyl)propanoic acid

: C27H28N2O6

Conditions

Conditions	Yield
With triethylamine In N,N-dimethyl-formamide at 20℃;

: 27167-53-9
N-(benzyloxycarbonyl)-D-alanine N-hydroxysuccinimide ester

: 184685-04-9
N-(N-benzyloxycarbonyl-D-alanyl)-p-bis(2-chloroethyl)amino-L-phenylalanine benzyl ester

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: 2.2 g / dioxane 2: 71 percent / SOCl2 / CHCl3 / 1) room temperature, 1 h, 2) 40-45 deg C, 2 h View Scheme

: 27167-53-9
N-(benzyloxycarbonyl)-D-alanine N-hydroxysuccinimide ester

: 144408-38-8
(2S,3S)-3--5-methylhexan-2-ol

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: 88 percent / dioxane / 12 h / Ambient temperature 2: 1.) (COCl)2, DMSO, 2.) Et3N / 1.) CH2Cl2, -78 deg C, 1 h, 2.) -78 deg C, 15 min 3: 1.) CuBr*S(CH3)2 / 1.) THF, ether, -78 deg C to -30 deg C, 2.) THF, -35 deg C, overnight View Scheme

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Dayang Chem (Hangzhou) Co.,Ltd.

Suzhou Health Chemicals Co., Ltd.

Research Peptide Biotechnology Co., Ltd.

Henan Allgreen Chemical Co.,Ltd

Antimex Chemical Limied

Henan Tianfu Chemical Co., Ltd.

ZHEJIANG JIUZHOU CHEM CO.,LTD

Jilin haofei import and export trade Co.,Ltd

ENAO Chemical Co, Limited

wuxi leji biology technology co., LTD

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Shanghai Apeptide Co., Ltd.

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INDOFINE Chemical Company, Inc.

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