Welcome to LookChem.com Sign In|Join Free

CAS

  • or
METHYL (S)-(-)-4-(TERT-BUTYLDIMETHYLSILYL) 2-METHYLPENTANOATE, a carboxylic acid ester, is an organic compound with a molecular formula of C13H26O2Si and a molecular weight of 242.42 g/mol. It features a chiral center and a tert-butyldimethylsilyl group, making it a valuable reagent in asymmetric synthesis and chiral separation techniques.

307532-01-0 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • Butanoic acid, 4-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-2-hydroxy-, methyl ester, (2S)-

    Cas No: 307532-01-0

  • No Data

  • No Data

  • No Data

  • SAGECHEM LIMITED
  • Contact Supplier
  • 307532-01-0 Structure
  • Basic information

    1. Product Name: METHYL (S)-(-)-4-(TERT-BUTYLDIMETHYLSIL&
    2. Synonyms: METHYL (S)-(-)-4-(TERT-BUTYLDIMETHYLSIL&;(S)-Methyl 4-((tert-butyldimethylsilyl)-oxy)-2-hydroxybutanoate
    3. CAS NO:307532-01-0
    4. Molecular Formula: C10H22O4Si
    5. Molecular Weight: 234.366
    6. EINECS: N/A
    7. Product Categories: Chiral Building Blocks;Esters;Organic Building Blocks
    8. Mol File: 307532-01-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 326.6°Cat760mmHg
    3. Flash Point: 180 °F
    4. Appearance: /
    5. Density: 0.979 g/mL at 25 °C(lit.)
    6. Vapor Pressure: 1.63E-05mmHg at 25°C
    7. Refractive Index: n20/D 1.493(lit.)
    8. Storage Temp.: 2-8°C
    9. Solubility: N/A
    10. CAS DataBase Reference: METHYL (S)-(-)-4-(TERT-BUTYLDIMETHYLSIL&(CAS DataBase Reference)
    11. NIST Chemistry Reference: METHYL (S)-(-)-4-(TERT-BUTYLDIMETHYLSIL&(307532-01-0)
    12. EPA Substance Registry System: METHYL (S)-(-)-4-(TERT-BUTYLDIMETHYLSIL&(307532-01-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany: 3
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 307532-01-0(Hazardous Substances Data)

307532-01-0 Usage

Uses

Used in Pharmaceutical Industry:
METHYL (S)-(-)-4-(TERT-BUTYLDIMETHYLSIL& is used as a building block for the synthesis of various organic compounds, particularly in the development of pharmaceuticals. Its chiral center and tert-butyldimethylsilyl group contribute to the creation of enantiomerically pure compounds, which are essential for the production of effective and safe drugs.
Used in Chemical Research:
In the field of chemical research, METHYL (S)-(-)-4-(TERT-BUTYLDIMETHYLSIL& serves as a valuable reagent for asymmetric synthesis and chiral separation techniques. Its unique structural features enable the development of novel methods and strategies for the synthesis of enantiomerically pure compounds, which are crucial in various chemical and biological applications.

Check Digit Verification of cas no

The CAS Registry Mumber 307532-01-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,7,5,3 and 2 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 307532-01:
(8*3)+(7*0)+(6*7)+(5*5)+(4*3)+(3*2)+(2*0)+(1*1)=110
110 % 10 = 0
So 307532-01-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H22O4Si/c1-10(2,3)15(4,5)14-7-6-8(11)9(12)13/h8,11H,6-7H2,1-5H3,(H,12,13)/t8-/m0/s1

307532-01-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl (2S)-4-[tert-butyl(dimethyl)silyl]oxy-2-hydroxybutanoate

1.2 Other means of identification

Product number -
Other names (2S)-4-TERT-BUTYLDIMETHYLSILYLOXY-2-HYDROXYBUTANOIC ACID METHYL ESTER

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:307532-01-0 SDS

307532-01-0Downstream Products

307532-01-0Relevant articles and documents

Synthesis of phenolic components of Grains of Paradise

Hattori, Hiroyuki,Mitsunaga,Clive, Derrick L.J.

, p. 1989 - 1991 (2019)

Two vanilloids, (5E)-8-(4-hydroxy-3-methoxyphenyl)oct-5-en-4-one (1) and 4-[3-hydroxydecyl]-2-methoxyphenol (2), isolated from the dried seeds of Grains of Paradise (Aframomum melegueta), were synthesized; the latter compound was made as the S-enantiomer and the material derived from the seeds was found to be a 1:1.7 mixture of the R and S isomers. The synthetic route used should allow the preparation of analogs having extended alkyl chains and consequently different lipophilicity, and 3, a homolog of 2, was also prepared.

ANTIMICROBIAL COMPOUNDS AND METHODS OF MAKING AND USING THE SAME

-

Paragraph 274; 275; 278-280, (2016/09/26)

The present disclosure relates generally to the field of antimicrobial compounds and to methods of making and using them. These compounds are useful for treating, preventing, reducing the risk of, and delaying the onset of microbial infections in humans a

ALKYNYL ALCOHOLS AND METHODS OF USE

-

, (2015/03/13)

The invention relates to compounds of Formula (0): wherein Q, A1-A8, R4 and R5 and each has the meaning as described herein. Compounds of Formula (0) and pharmaceutical compositions thereof are useful in the treatment of diseases and disorders in which undesired or over- activation of NF-kB signaling is observed.

Total synthesis of (-)-muricatacin

González, Maria,Gándara, Zoila,Covelo, Berta,Gómez, Generosa,Fall, Yagamare

supporting information; experimental part, p. 5983 - 5986 (2011/11/29)

A total synthesis of (-)-muricatacin has been achieved using a commercially available starting material and our furan approach to oxacyclic systems, the proven scope of which is thus broadened.

Synthesis of enantiomerically pure 2,5-disubstituted 3-oxygenated tetrahydrofurans

Alvarez, Carla,Perez, Manuel,Zuniga, Andrea,Gomez, Generosa,Fall, Yagamare

experimental part, p. 3883 - 3890 (2010/12/25)

The synthesis of enantiomerically pure 2,5-disubstituted 3-oxygenated tetrahydrofurans has been achieved from cheap and commercially available l-malic acid. This method was used to prepare an advanced intermediate toward CMI-977, a promising candidate for the treatment of chronic asthma. Georg Thieme Verlag Stuttgart · New York.

Total synthesis of ( - )-spirangien A, an antimitotic polyketide isolated from the myxobacterium Sorangium Cellulosum

Paterson, Ian,Findlay, Alison D.,Noti, Christian

experimental part, p. 594 - 611 (2010/04/23)

An expedient first total synthesis of (-)-spirangien A, a potent cytotoxic and antifungal polyketide of myxobacterial origin, is described. By using a common 1,3-diol intermediate obtained by an efficient aldol-reduction sequence for installation of the C

Vanadium-catalyzed asymmetric oxidation of α-hydroxy esters using molecular oxygen as stoichiometric oxidant

Radosevich, Alexander T.,Musich, Christine,Toste, F. Dean

, p. 1090 - 1091 (2007/10/03)

A vanadium-catalyzed method for the oxidative kinetic resolution of α-hydroxyesters, using oxygen as the terminal oxidant, is described. The catalyst is generated in situ from vanadium(V) tri-iso-propoxyoxide in combination with a tridentate ligand derived from 3,5-di-tert-butylsalicylaldehyde and (S)-tert-leucinol. The reaction allows for the enantioselective synthesis of both aromatic and aliphatic secondary alcohols, including those containing olefins and alkynes. Copyright

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 307532-01-0