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441788-45-0

(RS,S)-N-(3-hydroxy-1,3-diphenylpropylidene)-tert-butanesulfinamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 441788-45-0 Structure

  • Basic information

    1. Product Name: (RS,S)-N-(3-hydroxy-1,3-diphenylpropylidene)-tert-butanesulfinamide
    2. Synonyms: (RS,S)-N-(3-hydroxy-1,3-diphenylpropylidene)-tert-butanesulfinamide
    3. CAS NO:441788-45-0
    4. Molecular Formula:
    5. Molecular Weight: 329.463
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 441788-45-0.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: (RS,S)-N-(3-hydroxy-1,3-diphenylpropylidene)-tert-butanesulfinamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: (RS,S)-N-(3-hydroxy-1,3-diphenylpropylidene)-tert-butanesulfinamide(441788-45-0)
    11. EPA Substance Registry System: (RS,S)-N-(3-hydroxy-1,3-diphenylpropylidene)-tert-butanesulfinamide(441788-45-0)

  • 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: 441788-45-0(Hazardous Substances Data)

441788-45-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 441788-45-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,1,7,8 and 8 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 441788-45:
(8*4)+(7*4)+(6*1)+(5*7)+(4*8)+(3*8)+(2*4)+(1*5)=170
170 % 10 = 0
So 441788-45-0 is a valid CAS Registry Number.

441788-45-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (RS,S)-N-(3-hydroxy-1,3-diphenylpropylidene)-tert-butanesulfinamide

1.2 Other means of identification

Product number -
Other names -

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:441788-45-0 SDS

441788-45-0Relevant articles and documents

Development and application of a new general method for the asymmetric synthesis of syn- and anti-1,3-amino alcohols

Kochi, Takuya,Tang, Tony P.,Ellman, Jonathan A.

, p. 11276 - 11282 (2007/10/03)

A general method is described for asymmetric synthesis of both syn- and anti-1,3-amino alcohols. The first application of metalloenamines derived from N-sulfinyl imines is reported for the highly diastereoselective addition to aldehydes. The reduction of the product β-hydroxy N-sulfinyl imines 2 with catecholborane and LiBHEt3 provides syn- and anti-1,3-amino alcohols with very high diastereomeric ratios. This method was found to be effective for a variety of substrates incorporating either aromatic or various aliphatic substituents. The convergent and efficient asymmetric syntheses of the two natural products, (-)-8-epihalosaline and (-)-halosaline, were also accomplished.

Asymmetric synthesis of syn- and anti-1,3-amino alcohols

Kochi, Takuya,Tang, Tony P.,Ellman, Jonathan A.

, p. 6518 - 6519 (2007/10/03)

The first application of metalloenamines derived from N-sulfinyl imines is reported for the highly diastereoselective addition to aldehydes. Reduction of the β-hydroxy-N-sulfinyl imine products with catecholborane and LiBHEt3 provides syn- and

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