Cas 1026481-84-4,Benzoic acid (S)-3,3-difluoro-1-oxo-tetrahydro-1λ<sup>4</sup>-thiophen-2-ylmethyl ester

1026481-84-4

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Basic information

Product Name: Benzoic acid (S)-3,3-difluoro-1-oxo-tetrahydro-1λ⁴-thiophen-2-ylmethyl ester
Synonyms: Benzoic acid (S)-3,3-difluoro-1-oxo-tetrahydro-1λ⁴-thiophen-2-ylmethyl ester
CAS NO:1026481-84-4
Molecular Formula:
Molecular Weight: 274.288
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: Benzoic acid (S)-3,3-difluoro-1-oxo-tetrahydro-1λ⁴-thiophen-2-ylmethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Benzoic acid (S)-3,3-difluoro-1-oxo-tetrahydro-1λ⁴-thiophen-2-ylmethyl ester(1026481-84-4)
EPA Substance Registry System: Benzoic acid (S)-3,3-difluoro-1-oxo-tetrahydro-1λ⁴-thiophen-2-ylmethyl ester(1026481-84-4)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1026481-84-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1026481-84-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,6,4,8 and 1 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1026481-84:
(9*1)+(8*0)+(7*2)+(6*6)+(5*4)+(4*8)+(3*1)+(2*8)+(1*4)=134
134 % 10 = 4
So 1026481-84-4 is a valid CAS Registry Number.

1026481-84-4Upstream product

634181-98-9 (2S)-2-[(benzoyloxy)methyl]-3,3-difluorotetrahydrothiophene

1026481-84-4Downstream Products

1026481-84-4Relevant academic research and scientific papers

3-Deoxy-3,3-difluoro-D-arabinofuranose: First Stereoselective Synthesis and Application in Preparation of gem-Difluorinated Sugar Nucleosides

Zhang, Xingang,Xia, Hairong,Dong, XiCheng,Jin, Jing,Meng, Wei-Dong,Qing, Feng-Ling

, p. 9026 - 9033 (2007/10/03)

The design and synthesis of gem-difluorinated sugar nucleosides were described. The key intermediate, 3-deoxy-3,3-difluoro-D-arabinofuranose 9, was first stereoselectively prepared from the chiral gem-difluorohomoallyl alcohol 12. The kinetic formation of

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