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CAS

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101693-27-0

Propanoic acid, 2-(acetyloxy)-, 1,1-diMethylethyl ester, (R)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • Propanoic acid, 2-(acetyloxy)-, 1,1-dimethylethyl ester, (R)- (9CI)

    Cas No: 101693-27-0

  • USD $ 1.9-2.9 / Gram

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  • 101693-27-0 Structure

  • Basic information

    1. Product Name: Propanoic acid, 2-(acetyloxy)-, 1,1-diMethylethyl ester, (R)- (9CI)
    2. Synonyms: Propanoic acid, 2-(acetyloxy)-, 1,1-diMethylethyl ester, (R)- (9CI);Tert-butyl (R)-2-acetoxypropanoate
    3. CAS NO:101693-27-0
    4. Molecular Formula: C9H16O4
    5. Molecular Weight: 188.22094
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 101693-27-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 50 °C(Press: 0.1 Torr)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.020±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Propanoic acid, 2-(acetyloxy)-, 1,1-diMethylethyl ester, (R)- (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: Propanoic acid, 2-(acetyloxy)-, 1,1-diMethylethyl ester, (R)- (9CI)(101693-27-0)
    11. EPA Substance Registry System: Propanoic acid, 2-(acetyloxy)-, 1,1-diMethylethyl ester, (R)- (9CI)(101693-27-0)

  • 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: 101693-27-0(Hazardous Substances Data)

101693-27-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 101693-27-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,6,9 and 3 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 101693-27:
(8*1)+(7*0)+(6*1)+(5*6)+(4*9)+(3*3)+(2*2)+(1*7)=100
100 % 10 = 0
So 101693-27-0 is a valid CAS Registry Number.

101693-27-0SDS

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 2-Methyl-2-propanyl (2R)-2-acetoxypropanoate

1.2 Other means of identification

Product number -
Other names t-butyl (Z)-2-tosyloxy-vinyl ketone

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:101693-27-0 SDS

101693-27-0Downstream Products

101693-27-0Relevant articles and documents

ANTIHYPERTENSIVE COMPOUNDS

-

, (2008/06/13)

Antihypertensive compounds with angiotensin-converting enzyme inhibitory activity and diuretic activity are disclosed. Such compounds are useful in the treatment of cardiovascular disorders, especially hypertension and congestive heart failure, and are useful in the treatment of glaucoma.

Antiglaucoma agents

-

, (2008/06/13)

Pharmaceutical compositions and a method for reducing intraocular pressure by topically applying a carboxyalkyl dipeptide are disclosed.

ANTIHYPERTENSIVE COMPOUNDS HAVING BOTH DIURETIC AND ANGIOTENSIN CONVERTING ENZYME INHIBITORY ACTIVITY

-

, (2008/06/13)

Antihypertensive compounds with angiotensin-converting enzyme inhibitory activity and diuretic activity are disclosed. Such compounds are useful in the treatment of cardiovascular disorders, especially hypertension and congestive heart failure, and are us

STEREOSELEKTIVE SYNTHESE VON D-α-HYDROXYCARBONSAEUREN BZW. D-α-HYDROXYCARBONSAEUREN ENTHALTENDEN DEPSIPEPTIDEN AUS L-AMINOSAEUREN

Lerchen, Hans-Georg,Kunz, Horst

, p. 5257 - 5260 (2007/10/02)

Depsipeptides containing D-α-hydroxy carboxylic acids are efficiently synthesized by the reactions of L-α-halo-carboxylic acid esters (obtained from L-amino acids) with caesium salts of N-protected amino acids.

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