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13650-70-9

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13650-70-9 Usage

General Description

Tert-Butyl L-lactate is a chemical compound commonly used as a flavoring agent and fragrance ingredient in the food and cosmetic industries. It is a derivative of lactic acid, a naturally occurring organic acid, and is typically synthesized through the esterification of lactic acid with tert-butanol. Tert-Butyl L-lactate is known for its fruity and sweet odor and is often employed to enhance the aromatic profile of various products. Additionally, it is utilized as a solvent and as a starting material for the synthesis of other chemicals. Due to its low toxicity and pleasant scent, tert-Butyl L-lactate is widely utilized in a range of consumer goods and industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 13650-70-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,6,5 and 0 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 13650-70:
(7*1)+(6*3)+(5*6)+(4*5)+(3*0)+(2*7)+(1*0)=89
89 % 10 = 9
So 13650-70-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H14O3/c1-5(8)6(9)10-7(2,3)4/h5,8H,1-4H3/t5-/m0/s1

13650-70-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-Butyl L-lactate

1.2 Other means of identification

Product number -
Other names tert-Butyl (S)-(-)-lactate

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:13650-70-9 SDS

13650-70-9Relevant articles and documents

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Shemyakin,M.M. et al.

, (1966)

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Total Synthesis of (+)-Prunustatin A: Utility of Organotrifluoroborate-Mediated Prenylation and Shiina MNBA Esterification and Macrolactonization to Avoid a Competing Thorpe-Ingold Effect Accelerated Transesterification

Chojnacka, Maja W.,Batey, Robert A.

supporting information, p. 5671 - 5675 (2018/09/13)

A convergent total synthesis of (+)-prunustatin A is described through the assembly of two key fragments and a macrolactonization. Shiina MNBA couplings were used for the formation of each of the four ester bonds in the tetralactone ring, including the key macrocyclization which was essential to minimize competing Thorpe-Ingold accelerated transesterification. Other key steps included an organoboron-based prenylation using potassium prenyltrifluoroborate and a carbonyldiimidazole-mediated coupling to form the salicylamide.

METHODS AND COMPOSITIONS FOR PREVENTING OPIOID ABUSE

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Paragraph 0705; 0708, (2016/11/28)

Abuse-resistant opioid compounds, drug delivery systems, pharmaceutical compositions comprising an opioid covalently bound to a chemical moiety are provided. Methods of delivering an active ingredient to a subject and methods of preventing opioid abuse are also provided.

Total synthesis of carolacton, a highly potent biofilm inhibitor

Schmidt, Thomas,Kirschning, Andreas

supporting information; experimental part, p. 1063 - 1066 (2012/03/11)

Metals are the key players in the synthesis of caralacton, a strong inhibitor of bacterial biofilms. The total synthesis is based on several metal-mediated key transformations such as the Ley and the Duthaler-Hafner aldol reactions, the Marshall reaction and Breit's substitution, as well as the Nozaki-Hiyama-Kishi and Negishi-Fu C-C coupling reactions. Copyright

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