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1307857-46-0

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1307857-46-0 Usage

Type of compound

Diethyl ester of 2,2-difluoro-4-methylenepentanedioic acid

Usage

Intermediate in organic synthesis

Importance

Production of various pharmaceuticals and agrochemicals

Chemical properties

Versatile

Physical state

Colorless liquid

Odor

Mild, fruity

Solubility

Soluble in most organic solvents

Additional uses

Production of polymers, reagent in organic reactions

Check Digit Verification of cas no

The CAS Registry Mumber 1307857-46-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,0,7,8,5 and 7 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1307857-46:
(9*1)+(8*3)+(7*0)+(6*7)+(5*8)+(4*5)+(3*7)+(2*4)+(1*6)=170
170 % 10 = 0
So 1307857-46-0 is a valid CAS Registry Number.

1307857-46-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Diethyl 2,2-difluoro-4-methylenepentanedioate

1.2 Other means of identification

Product number -
Other names (3aR,4S,7R,7aS)-Hexahydro-2,2,4-trimethyl-1,3-dioxolo[4,5-c]pyridin-7-ol

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:1307857-46-0 SDS

1307857-46-0Relevant articles and documents

SAR insights into TET2 catalytic domain inhibition: Synthesis of 2-Hydroxy-4-Methylene-pentanedicarboxylates

Tiwari, Anand D.,Guan, Yihong,Grabowski, Dale R.,Maciejewski, Jaroslaw P.,Jha, Babal K.,Phillips, James G.

, (2021)

The TET (Ten-Eleven Translocation) dioxygenase enzyme family comprising 3 members, TET1-3, play key roles in DNA demethylation. These processes regulate transcription programs that determine cell lineage, survival, proliferation, and differentiation. The impetus for our investigations described here is derived from the need to develop illuminating small molecule probes for TET enzymes with cellular activity and specificity. The studies were done so in the context of the importance of TET2 in the hematopoietic system and the preponderance of loss of function somatic TET2 mutations in myeloid diseases. We have identified that 2-hydroxy-4-methylene-pentanedicarboxylic acid 2a reversibly competes with the co-substrate α-KG in the TET2 catalytic domain and inhibits the dioxygenase activity with an IC50 = 11.0 ± 0.9 μM at 10 μM α-KG in a cell free system and binds in the TET2 catalytic domain with Kd = 0.3 ± 0.12 μM.

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