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412912-89-1

(S)-3-((tert-butyldimethylsilyl)oxy)-3-phenylpropanal is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 412912-89-1 Structure

  • Basic information

    1. Product Name: (S)-3-((tert-butyldimethylsilyl)oxy)-3-phenylpropanal
    2. Synonyms: (S)-3-((tert-butyldimethylsilyl)oxy)-3-phenylpropanal
    3. CAS NO:412912-89-1
    4. Molecular Formula:
    5. Molecular Weight: 264.44
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 412912-89-1.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: (S)-3-((tert-butyldimethylsilyl)oxy)-3-phenylpropanal(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-3-((tert-butyldimethylsilyl)oxy)-3-phenylpropanal(412912-89-1)
    11. EPA Substance Registry System: (S)-3-((tert-butyldimethylsilyl)oxy)-3-phenylpropanal(412912-89-1)

  • 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: 412912-89-1(Hazardous Substances Data)

412912-89-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 412912-89-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,1,2,9,1 and 2 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 412912-89:
(8*4)+(7*1)+(6*2)+(5*9)+(4*1)+(3*2)+(2*8)+(1*9)=131
131 % 10 = 1
So 412912-89-1 is a valid CAS Registry Number.

412912-89-1Relevant articles and documents

A designed amide as an aldol donor in the direct catalytic asymmetric aldol reaction

Weidner, Karin,Kumagai, Naoya,Shibasaki, Masakatsu

, p. 6150 - 6154 (2014)

The direct catalytic asymmetric aldol reaction offers efficient access to β-hydroxy carbonyl entities. Described is a robust direct catalytic asymmetric aldol reaction of α-sulfanyl 7-azaindolinylamide, thus affording both aromatic and aliphatic β-hydroxy amides with high ee values. The design of this transformation features a cooperative interplay of a soft and a hard Lewis acid, which together facilitate the challenging chemoselective enolization by a hard Bronsted base.

Confinement-Controlled, Eithersyn- oranti-Selective Catalytic Asymmetric Mukaiyama Aldolizations of Propionaldehyde Enolsilanes

Amatov, Tynchtyk,Tsuji, Nobuya,Maji, Rajat,Schreyer, Lucas,Zhou, Hui,Leutzsch, Markus,List, Benjamin

supporting information, p. 14475 - 14481 (2021/09/13)

Protected aldols (i.e., true aldols derived from aldehydes) with eithersyn- oranti- stereochemistry are versatile intermediates in many oligopropionate syntheses. Traditional stereoselective approaches to such aldols typically require several nonstrategic

A flexible enantioselective synthesis of (+)-centrolobine and 5-epi-diospongin-A using asymmetric transfer hydrogenation/tandem Grubbs cross-metathesis/oxy-Michael reaction as key steps

Kumaraswamy, Gullapalli,Rambabu, Dasa

, p. 196 - 201 (2013/04/10)

An efficient enantioselective synthesis of (+)-centrolobine and 5-epi-diospongin-A was achieved by the use of asymmetric transfer hydrogenation (ATH)/tandem Grubbs cross-metathesis/oxy-Michael reaction. Furthermore, this strategy allows for diastereodiver

A short and efficient synthesis of (-)-diospongin A

Bressy, Cyril,Allais, Florent,Cossy, Janine

, p. 3455 - 3456 (2007/10/03)

The synthesis of (-)-diospongin A has been achieved from benzaldehyde in six steps with an overall yield of 29%. Georg Thieme Verlag Stuttgart.

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