Welcome to LookChem.com Sign In|Join Free
  • or
(S)-(-)-2-ISOCYANATOGLUTARIC ACID DIETHYL ESTER is a chemical compound with an isocyanate functional group, derived as a diethyl ester of isocyanatoglutaric acid. It is recognized for its reactivity and unique structure, making it a versatile intermediate in the synthesis of a range of organic compounds.

145080-95-1

Post Buying Request

145080-95-1 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

145080-95-1 Usage

Uses

Used in Polymer Production:
(S)-(-)-2-ISOCYANATOGLUTARIC ACID DIETHYL ESTER is used as a monomer or a reactive intermediate for the production of polymers. Its isocyanate group facilitates the formation of polyurethanes and other polymeric materials, which are known for their durability and versatility in various applications.
Used in Adhesive and Coating Industries:
In the adhesive and coating industries, (S)-(-)-2-ISOCYANATOGLUTARIC ACID DIETHYL ESTER is used as a component in formulating strong and durable adhesives and coatings. Its reactive nature allows for the creation of robust bonds and protective layers on various surfaces.
Used in Pharmaceutical Manufacturing:
(S)-(-)-2-ISOCYANATOGLUTARIC ACID DIETHYL ESTER is utilized as an intermediate in the synthesis of pharmaceuticals. Its unique chemical structure contributes to the development of new drug molecules, potentially leading to advancements in medicinal chemistry.
Used in Agrochemical Development:
(S)-(-)-2-ISOCYANATOGLUTARIC ACID DIETHYL ESTER is also used in the agrochemical sector, where it serves as a building block for the synthesis of pesticides and other agrochemicals. Its reactivity and functional groups are harnessed to create effective and targeted products for agricultural use.
Used in Organic Chemistry Research:
Due to its distinctive structure and functional groups, (S)-(-)-2-ISOCYANATOGLUTARIC ACID DIETHYL ESTER holds potential for further research and development in organic chemistry. It can be explored for new reactions, mechanisms, and applications, contributing to the expansion of chemical knowledge and innovation.

Check Digit Verification of cas no

The CAS Registry Mumber 145080-95-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,0,8 and 0 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 145080-95:
(8*1)+(7*4)+(6*5)+(5*0)+(4*8)+(3*0)+(2*9)+(1*5)=121
121 % 10 = 1
So 145080-95-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H15NO5/c1-3-15-9(13)6-5-8(11-7-12)10(14)16-4-2/h8H,3-6H2,1-2H3/t8-/m0/s1

145080-95-1 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • TCI America

  • (I0468)  Diethyl (S)-(-)-2-Isocyanatoglutarate  >97.0%(GC)

  • 145080-95-1

  • 1g

  • 890.00CNY

  • Detail
  • TCI America

  • (I0468)  Diethyl (S)-(-)-2-Isocyanatoglutarate  >97.0%(GC)

  • 145080-95-1

  • 5g

  • 2,650.00CNY

  • Detail

145080-95-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name diethyl (2S)-2-isocyanatopentanedioate

1.2 Other means of identification

Product number -
Other names (S)-(-)-2-Isocyanatopentanedioic Acid Diethyl 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:145080-95-1 SDS

145080-95-1Relevant academic research and scientific papers

Synthesis process of Raltitrexed key intermediate

-

Paragraph 0047-0051, (2019/05/22)

The invention relates to the technical field of medicine preparation, in particular to a synthesis process of a Raltitrexed key intermediate. According to the synthesis process of the Raltitrexed keyintermediate, forming an active intermediate (isocyanate) through glutamate diethyl ester, the active intermediate and N-methyl-(2-thienyl) tert-butyl carbamate are directly reacted, and a target product N-[5-[N-(t-butyloxycarboryl)-N-methyl amino]-2-thenoyl]-L-glutamate diethyl ester is prepared by two steps. The synthesis process avoids difficulties of potential risks of part of racemization ofa chiral center caused by amidation reaction, low yield, complicated operation and purification and the like. The synthesis process of the Raltitrexed key intermediate is simple to operate, short in line, environmentally friendly and high in yield.

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 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 145080-95-1