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(2S)-3-benzyloxy-2-<(benzyloxycarbonyl)amino>propanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 58578-42-0 Structure
  • Basic information

    1. Product Name: (2S)-3-benzyloxy-2-<(benzyloxycarbonyl)amino>propanol
    2. Synonyms: (2S)-3-benzyloxy-2-<(benzyloxycarbonyl)amino>propanol
    3. CAS NO:58578-42-0
    4. Molecular Formula:
    5. Molecular Weight: 315.369
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 58578-42-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (2S)-3-benzyloxy-2-<(benzyloxycarbonyl)amino>propanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2S)-3-benzyloxy-2-<(benzyloxycarbonyl)amino>propanol(58578-42-0)
    11. EPA Substance Registry System: (2S)-3-benzyloxy-2-<(benzyloxycarbonyl)amino>propanol(58578-42-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 58578-42-0(Hazardous Substances Data)

58578-42-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58578-42-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,5,7 and 8 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 58578-42:
(7*5)+(6*8)+(5*5)+(4*7)+(3*8)+(2*4)+(1*2)=170
170 % 10 = 0
So 58578-42-0 is a valid CAS Registry Number.

58578-42-0Relevant articles and documents

Enantioselective Friedel-Crafts reactions between phenols and N-tosylaldimines catalyzed by a leucine-derived bifunctional catalyst

Li, Guo-Xing,Qu, Jin

supporting information; experimental part, p. 5518 - 5520 (2012/07/01)

Enantioselective Friedel-Crafts reactions between phenols and N-tosylaldimines were developed using a bifunctional catalyst readily prepared from l-leucine. The chiral benzylic amine products were obtained in high yields (up to 96% yield) and good to high enantiomeric excesses (up to 95% ee).

Trimethylsilyl trifluoromethanesulfonate (TMSOTf) assisted facile deprotection of N,O-acetonides

Poon, Kevin W. C.,Lovell, Kimberly M.,Dresner, Kendra N.,Datta, Apurba

, p. 752 - 755 (2008/09/18)

(Chemical Equation Presented) Employing TMSOTf as an easily available reagent, we have developed a mild and efficient method for the deprotection of both terminal and internal N,O-acetonide functionalities. Various regularly used protecting groups and com

Synthesis and evaluation of arylaminoethyl amides as noncovalent inhibitors of cathepsin S. Part 3: Heterocyclic P3

Tully, David C.,Liu, Hong,Alper, Phil B.,Chatterjee, Arnab K.,Epple, Robert,Roberts, Michael J.,Williams, Jennifer A.,Nguyen, Khanhlinh T.,Woodmansee, David H.,Tumanut, Christine,Li, Jun,Spraggon, Glen,Chang, Jonathan,Tuntland, Tove,Harris, Jennifer L.,Karanewsky, Donald S.

, p. 1975 - 1980 (2007/10/03)

A series of Nα-2-benzoxazolyl-α-amino acid-(arylaminoethyl)amides were identified as potent, selective, and noncovalent inhibitors of cathepsin S. Structure-activity relationships including strategies for modulating the selectivities among cathepsins S, K, and L, and in vivo pharmacokinetics are discussed. A X-ray structure of compound 3 bound to the active site of cathepsin S is also reported.

Convenient preparation of O-benzyl-N-Cbz-D-serinol, an intermediate in β-hydroxy-α-amino acid synthesis

Monache,Di Giovanni,Maggio,Misiti,Zappia

, p. 1155 - 1158 (2007/10/02)

A convenient preparation of (2S)-3-benzyloxy-2-[(benzyloxycarbonyl)amino]propanol (2) in 52% yield, employing cheap L-serine as starting material, is described. Conversion of 2 into methyl (2Z,4R)-5-benzyloxy-4-[(benzyloxycarbonyl)amino]pent-2-enoate (1) is reported.

Synthesis and platelet-activating factor (PAF)-antagonistic activities of trisubstituted piperazine derivatives

Fukushi,Mabuchi,Terashita,Nishikawa,Sugihara

, p. 551 - 559 (2007/10/02)

2- or 3-Substituted 1-(2,3-dimethoxy-6,7-dihydro-5H-benzocyclobepten-8- ylcarbonyl)-4-(3,4,5-trimethoxybenzoyl)- and 4-(3,4,5- trimethoxybenzyl)piperazines (2a - s, 3a, b) were prepared and evaluated for antagonistic activities against platelet-activating

Pinacol cross coupling of 2-[N-(alkoxycarbonyl)amino] aldehydes and aliphatic aldehydes by [V2Cl3(THF)6]2[Zn2Cl 6]. Synthesis of syn,syn-3-[N-(alkoxycarbonyl)amino] 1,2-diols

Konradi, Andrei W.,Kemp, Scott J.,Pedersen, Steven F.

, p. 1316 - 1323 (2007/10/02)

Slow addition of 2-[N-(alkoxycarbonyl)amino] aldehydes to mixtures of [V2Cl3(THF)6]2[Zn2Cl 6] and aliphatic aldehydes gave syn,syn-3-[N-(alkoxycarbonyl)amino] 1,2-diols in good yield and high enantiomeric purity (>99:1). The alkyl group of the N-alkoxycarbonyl was shown to influence the yield: Me > allyl > Bn > t-Bu. Only the syn,syn diastereomer was observed (>20:1), except with N-Cbz-alaninal (10:1:1), O-benzyl-N-Cbz-serinal (7:1), and N-Cbz-prolinal (5:1 to 12:1). A new serinai derivative, N-Cbz-O-TBS-serinal, was cross coupled with n-pentadecanal to give a derivative of xylo-D-C18-phytosphingosine.

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